Table 1 The aggregated characteristics of the included RCTs.
Source | Study design | Population | Treatment | Outcome measures | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
No. of arm | Diagnosis criteria | No | Age | Intervention Group (type; duration; frequency; or drug name; dose; duration; frequency) | Comparator Group (type; duration; frequency; or drug name; dose; duration; frequency) | Third Group (type; duration; frequency; or drug name; dose; duration; frequency) | ||||||
Ai et al.23 | 2018 | 2 | DSM-V | I: 50; C: 50 | I: 20.1 ± 3.6; C: 20.2 ± 3.5 | MA + paroxetine | MA: 1 time/ d, 6 w; paroxetine: 20 mg/time, 1 time/ d, 6 w | Paroxetine | 20 mg/time, 1 time/ d, 6 w | N/A | N/A | HAMD-17(0, 1, 2, 4, 6 w); response rates |
Allen et al.24 | 2006 | 3 | DSM-IV | I: 53; C: 52; T: 52 | I: 23.3 ± 11.4; C:24.6 ± 12.8; T: 22.7 ± 14.0 | MA | 2 times/ w for first 4 w, 1 time/ w for another 4 w, 8 w | MA | 2 times/ w for first 4 w, 1 time/ w for another 4 w, 8 w | Wait-list | 8w | HAMD-17 (0, 4, 8, 12, 16 w), BDI (0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 w); response rates (8, 16 w), remission rates (8, 16 w) |
Chen et al.25 | 2014 | 2 | ICD-10 | I: 40; C: 33 | I: 36.2 ± 11.7; C: 35.0 ± 10.5 | MA + Paroxetine | MA: 3 times/ w, 6 w; Paroxetine: 1 time/ d, 10–20 mg/ time, 6 w | Paroxetine | 1 time/ d, 10–20 mg/ time, 6 w | N/A | N/A | HAMD-17(0, 1, 2, 4, 6w), SERS( 2, 4, 6w); response rates |
Chen et al.26 | 2010 | 2 | CCMD-III | I: 33; C: 30 | I:65.30 ± 3.592; C: 65.10 ± 3.736 | MA | 5 time/ w, 6 w | Fluoxetine | 1 time/ d, 20 mg/ time, 6 w | N/A | N/A | HAMD(0, 2, 4, 6w); response rates |
Chen et al.27 | 2011 | 2 | CCMD-III | I: 30; C: 30 | I: 43.9 ± 11.2; C: 49.0 ± 13.4 | EA + Fluoxetine | EA: 6 times/ w, 8 w; Fluoxetine: 1 time/ d, 20 mg/ time, 8 w | Fluoxetine | 1 time/ d, 20 mg/ time, 8 w | N/A | N/A | HAMD-17(0, 1, 4, 8 w); response rates |
Dong et al.28 | 2017 | 2 | CCMD-III | I: 30; C: 30 | I: 15.6 ± 1.40; C: 14.9 ± 1.45 | MA + Psychotherapy | MA: 1 time/ d, 10 d one session, another session after 2d, 30 d; Psychotherapy: 1 times/ w, 4 w | Sertraline + Psychotherapy | Sertraline: 1 time/ d, 50 mg/ time, 30 d; Psychotherapy: : 1 times/ w, 4 w | N/A | N/A | HAMD-24(0, 10, 20, 30d) |
Duan et al.29 | 2008 | 3 | CCMD-III | I: 25; C: 25; T: 25 | I: 50.12 ± 4.32; C: 49.72 ± 5.47; T: 48.93 ± 7.60 | EA | 6 time/ w, 6 w | Fluoxetine | 20 mg/ d, 6 w | EA + Fluoxetine | EA: 6 time w, 6 w; Fluoxetine: 20 mg/ d, 6 w | HAMD(0, 6w), TESS (2, 4, 6w); response rates |
Feng et al.30 | 2015 | 3 | ICD-10 | I: 60; C: 60; T: 60 | I: 36.4 ± 9.9; C: 37.1 ± 9.8; T: 36.6 ± 10.0 | MA + SSRIs | MA: 3 times/ w, 6 w; Fluoxetine: 20–60 mg/ d; or Paroxetine: 20–60 mg/ d; or Citalopram: 20–60 mg/ d; or Sertraline: 50–200 mg/ d; or Fluvoxamine: 50–300 mg/d; 1–2 times/ d, 6w | SSRIs | Fluoxetine: 20–60 mg/ d; or Paroxetine: 20–60 mg/ d; or Citalopram: 20–60 mg/ d; or Sertraline: : 50–200 mg/ d; or Fluvoxamine: 50–300 mg/d; 1–2 times/ d, 6w | HC | HC | MADRS(0, 1, 2, 4, 6w); SERS(1, 2, 4, 6w) |
Gallagher et al.31 | 2001 | 3 | DSM-IV | 38 | 18–45 | MA | 8 w | MA | 8 w | Wait-list | 8 w | HRSD-19(0, 8 w) |
Gu et al.32 | 2015 | 2 | CCMD-III | I: 30; C: 30 | I: 61.83 ± 10.33; C: 63.53 ± 10.11 | MA | 1 time/ d, 30 d | Fluoxetine | 1 time/ d, 20 mg/ time, 30 d | N/A | N/A | HAMD-17(0, 30d) |
Guo et al33 | 2019 | 2 | CCMD-3 | I: 22; C: 22 | I: 40.86 ± 9.84; C: 42.09 ± 10.71 years | MA + Fluoxetine | MA: 1 time/ d, 3w; Fluoxetine: 20 mg/ time,1 time/ d, 3 W | Fluoxetine | 20 mg/ time,1 time/ d, 3 W | N/A | N/A | HAMD-17, PHQ-9(0, 3w); response rate |
Han et al34 | 2019 | 2 | DSM-V | I: 25; C: 25 | I: 37.0 (32. 0, 41. 5); C: 39.0 (35.0, 46.5) | EA | 3 times/ w, 6 w | MA | 3 times/ w, 6 w | N/A | N/A | HAMD, SDS(0,6w); response rate |
Huang et al.35 | 2013 | 2 | CCMD-III | I: 30; C: 30 | I: 49.25 ± 14.03; C: 50.78 ± 12.96 | MA + Paroxetine | MA: 3 times/ w, 6 w; Paroxetine: 1 time/ d, 20–40 mg/ time, 6 w | Paroxetine | 1 time/ d, 20–40 mg/ time, 6 w | N/A | N/A | HAMD(0, 1, 6w), SDS(0, 1, 6w); Asberg(1, 6w); response rates |
Jiang et al.36 | 2008 | 2 | CCMD-III | I: 34; C: 34 | I: 36.4 ± 11.7; C: 35.6 ± 13.1 | MA + Citalopram | MA: 1 time/ 2 d, 40 d Citalopram: 20 mg/ d, 1 time/ d, 40 d | Citalopram | 20 mg/ d, 1 time/ d, 40 d | N/A | N/A | HAMD-17(0, 1, 2, 4, 6w), CGI-SI(0, 2, 4, 6w); TESS; response rates |
Li et al.37 | 2013 | 2 | DSM-IV | I: 62; C: 62 | I: 33.9 ± 12.0; C: 34.8 ± 12.4 | EA + Sertraline | EA: 6 times/ w, 8 w; Sertraline: 50–100 mg/ d, 8 w | Sertraline | 50–100 mg/d, 8 w | N/A | N/A | HAMD-17(0, 1, 2, 4, 8w) |
Li et al.38 | 2004 | 3 | CCMD-III | I: 30; C: 30; T: 50 | I: 41.8 ± 14.6; C: 39.4 ± 13.4; T: 45.8 ± 14.5 | MA | 5 times/ w, 6 w | Fluoxetine | 1 time/ d, 20 mg/ time, 6 w | MA 2 | 5 times/ w, 6 w | HRSD, SDS(0, 6 w); response rates |
Lin et al.39 | 2004 | 2 | CCMD-III | I: 29; C: 28 | I: 40.3 ± 11.5; C: 44.6 ± 12.7 | MA + Paroxetine | MA: 1 time/ d, 5 time/ w, 6 w; Paroxetine: 1 time/ d, 10 mg/ time, 6 w | Paroxetine | 1 time/ d, 20 mg/ time, 6 w | N/A | N/A | HAMD-17(0, 1, 2, 4, 6w), HAMA(0, 1, 2, 4, 6w); CGI TESS; response rates |
Li et al.40 | 2017 | 2 | ICD-10, CCMD-III | I: 30; C: 30 | I: 34 ± 8; C:35 ± 8 | MA + Paroxetine | MA: 6 time/ w, 8 w; Paroxetine: 10- 20 mg/ time, 1 time/ d, 8w | Paroxetine | 10- 20 mg/ time, 1 time/ d, 8w | N/A | N/A | HAMD-17(0,1,2,3,4,5,6,7,8w); response rates |
Lin et al.41 | 2005 | 2 | CCMD-III | I: 30; C: 23 | I: 41.7 ± 12.1; C: 43.1 ± 11.5 | MA + Fluoxetine | MA: 5 time/ w, 6 w; Fluoxetine: 1 time/ d, 20 mg/ time, 6 w | Fluoxetine | 1 time/ d, 20 mg/ time, 6 w | N/A | N/A | HAMD-17(0, 1, 2, 4, 6w), HAMA(0, 1, 2, 4, 6w); CGI, TESS; response rates |
Lin et al.42 | 2014 | 2 | CCMD-III | I: 61; C: 61 | NR | MA + Fluoxetine | 1 time/ d, 5 time/ w, 4 w | Fluoxetine | 1 time/ d, 20 mg/ time, 4 w | N/A | N/A | HAMD-17(0, 1, 2, 4w), SDS(0, 4w ); response rates |
Liu et al.43 | 2018 | 2 | ICD-10 | I: 21; C: 21 | I: 44 ± 10; C:43 ± 9 | Fluoxetine + MA | MA: 1 time/ d for first 3d, then once every 3d, 8 w; Fluoxetine: 10 mg, 1 time/ d, 8w | Fluoxetine + Sham MA | Sham MA: 1 time/ d for first 3d, then once every 3d, 8 w; Fluoxetine: 10 mg, 1 time/ d, 8w | N/A | N/A | MADRS(0, 4, 8w), SDS(0, 4, 8w); response rates |
Liu et al.44 | 2005 | 2 | CCMD-III | I: 21; C: 20 | I: 48.9 ± 12.0; C: 49.0 ± 13.4 | EA + SSRIs* | EA: 6 w; SSRIs: 6 w* | SSRIs* | SSRIs: 6 w* | N/A | N/A | HAMD-17(0, 1, 2, 4, 6w) |
Liu et al.45 | 2014 | 3 | CCMD-III | I: 45; C: 45; T: 45 | I: 47.11 ± 8.32; C:47.58 ± 8.21; T: 48.11 ± 7.97 | MA + SSRIs | MA: 1 time/ 2 d, 4 w; Fluoxetine: 20 ~ 60 mg/ d; or Paroxetine: 20–60 mg/ d; or Citalopram: 20–10 mg/ d; or Sertraline: 50–200 mg/ d; 1time/ d, 4 w | SSRIs | Fluoxetine: 20 ~ 60 mg/ d; or Paroxetine: 20–60 mg/ d; or Citalopram: 20–10 mg/ d; or Sertraline: 50–200 mg/ d; 1time/ d, 4 w | HC | HC | HAMD-17(0, 1, 2, 4w), SERS(1, 2, 4w); response rates |
Liu et al.46 | 2015 | 2 | CCMD-III | I: 45; C: 45; T: 45 | I: 36 ± 11; C: 37 ± 11; T: 36 ± 11 | MA + SSRIs | MA: 1 time/ 2 d, 4 w; SSRI: Fluoxetine: 20–60 mg/ d; or Paroxetine: 20–60 mg/ d; or Citalopram: 20–60 mg/ d; or Sertraline: 50–200 mg/ d; or Fluvoxamine: 50–300 mg/d; 1–2 times/ d, 4 w | SSRIs | Fluoxetine: 20 ~ 60 mg/ d; or Paroxetine: 20–60 mg/ d; or Citalopram: 20–60 mg/ d; or Sertraline: 50–200 mg/ d; or Fluvoxamine: 50–300 mg/d; 1-2times/ d, 4 w | HC | HC | HAMD-17(0, 1, 2, 4w) |
Liu et al.47 | 2017 | 3 | ICD-10 | I: 47; C: 48; T: 45 | I: 47.11 ± 9.10; C:47.27 ± 9.03; T:47.18 ± 9.21 | MA + Venlafaxine | MA: 5 times/ w, 8w; Venlafaxine: 75–225 mg/ d, 8w | Venlafaxine | 75–225 mg/ d, 8w | HC | HC | HAMD-17(0, 8w) |
Lu et al.48 | 2017 | 2 | CCMD-III | I: 30; C: 30 | I:52.7 ± 17.4; C:56.7 ± 16.3 | MA + Escitalopram | EA: 3 times/ w, 2 w; Escitalopram :20 mg, 1 time/ d, 2w | Escitalopram | 20 mg, 1 time/ d, 2w | N/A | N/A | HAMD(0, 1, 2w), |
Luo et al.49 | 2003 | 3 | DSM-IV | I: 31; C: 32; T: 32 | I: 30 ± 11; C: 34 ± 13; T: 32 ± 12 | EA + Placebo | EA: 1 time/ d, 5 time/ w; Placebo: 1 time/ d, 20 mg/ time | Fluoxetine + Sham EA | Fluoxetine: 1 time/ d, 20 mg/ time; Sham EA: 1 time/ d, 5 time/w | Placebo + sham-EA | Placebo: 1 time/ d, 20 mg/ time; sham-EA: 1 time/ d, 5 time/ w | HAMD, SDS, CGI(0, 2, 4, 6w); Asberg(0, 6w) |
Ma et al.50 | 2011 | 2 | CCMD-III | I: 31; C: 29 | I: 51.1 ± 12.85; C:50.9 ± 11.29 | MA | 5 time/ w, 6 w | Fluoxetine | 1 time/ d, 20 mg/ time, 6 w | N/A | N/A | HAMD-17(0, 2, 4, 6w), Asberg(2, 4, 6w); response rates |
Ma et al.51 | 2011 | 2 | ICD-10 | I: 26; C: 29 | I: 46.27 ± 13.13 C: 40.52 ± 14.21 | EA + Paroxetine | EA: 3 times/ w, 6w; Paroxetine: 10–20 mg/ d, 1times/ d, 6w | Paroxetine | 10–20 mg/ d, 1times/ d, 6w | N/A | N/A | HAMD-17, SERS(0, 1, 2, 4, 6w), CGI(0, 6 w) |
Ma et al.52 | 2011 | 2 | ICD-10 | I: 26; C: 29 | I: 46.27 ± 13.13 C: 40.52 ± 14.21 | EA + Paroxetine | EA: 3 times/ w, 6 w; Paroxetine: 10–20 mg/ d, 1 time/ d, 6w | Paroxetine | 10–20 mg/ d, 1 time/ d, 6w | N/A | N/A | HAMD-17, SDS(0, 1, 2, 4, 6w) |
Ma et al53 | 2020 | 2 | CCMD-3/DSM-V | I: 30; C: 32 | 22–70 | MA | 3 times/ w, 8w | Sham MA | 3 times/ w, 8w | N/A | N/A | HAMD, SDS, TESS(0, 4, 8,12w) |
Pei et al.54 | 2006 | 2 | CCMD-III | I: 62; C: 58 | I: 18–61; C:20–64 | MA | 5 time/ w, 6 w | Fluoxetine | 1 time/ d, 20 mg/ time, 6 w | N/A | N/A | HAMD(0, 2, 4, 6w); response rates |
Qu et al.55 | 2013 | 3 | ICD-10 | I: 58; C: 54; T: 48 | I: 33.2 ± 9.0; C: 32.3 ± 9.6; T: 34.4 ± 10.8 | EA + Paroxetine | EA: 3 times/ w, 6 w; Paroxetine:10–20 mg/ d, 6 w | MA + Paroxetine | MA: 3 times/ w, 6 w; Paroxetine:10–20 mg/ d, 6 w | Paroxetine | Paroxetine:10–20 mg/ d, 6 w | HAMD-17 (0, 1, 2, 4, 6w, 10w follow-up), SDS (0, 1, 2, 4, 6w, 10w follow-up), CGI-S (0, 1, 2, 4, 6w, 10w follow-up); response rates |
Roschke et al.56 | 2000 | 3 | DSM-III-R | I: 22; C: 24; T: 24 | I: 49 ± 13; C: 47 ± 9; T: 49 ± 11 | MA + Mianserin | MA: 3 times/ w, 4 w; Mianserin: 90–120 mg/ d, 4 w ; | Sham MA + Mianserin | Mianserin: 90–120 mg/ d, 4 w; Sham MA: 3 times/ w, 4 w | Mianserin | 90–120 mg/ d, 4 w | GAS, BRMS, CGI, Bf-S (twice/ w for 8 w); response rates |
Shi et al.57 | 2015 | 3 | CCMD-III | I: 30; C: 30; T: 30 | I: 52.33 ± 9.93; C: 48.46 ± 8.44; T: 49.94 ± 9.41 | MA | 5 times/ w, 8 w | MA | 5 times/ w, 8 w | Fluoxetine | 1 time/ d, 20 mg/ time, 8 w | HAMD-17(0, 4, 8w); response rates |
Song et al.58 | 2013 | 2 | CCMD-III | I: 30; C: 30 | I: 42.32 ± 12.47; C: 43.74 ± 12.52 | MA | 6 times/ w, 6 w | Fluoxetine | 1 time/ d, 20 mg/ time, 6 w | N/A | N/A | HAMD(0, 2, 4, 6w), Asberg (2, 4, 6w); response rates |
Sun et al.59 | 2012 | 2 | CCMD-III | I: 20; C: 20 | I: 32.5 ± 10.3; C: 31.5 ± 11.4 | EA + Venlafaxine | EA: 5 times/ w, 2 w; Venlafaxine: 1 time/ d, 75–150 mg/ time, 2 w | Venlafaxine | 1 time/ d, 75–150 mg/ time, 2 w | N/A | N/A | HAMD(0, 1, 2w); TESS; response rates |
Sun et al.60 | 2013 | 3 | DSM-IV | I: 25; C: 25; T: 25 | I: 43.10 ± 13.86; C:42.56 ± 10.70; T:40.72 ± 12.80 | EA | 5 times/ w, 6 w | EA | 5 times/ w, 6 w | Fluoxetine | 20 mg/ d, 6 w | HDRS-24 (0, 2, 4, 6 w) |
Tang et al.61 | 2003 | 2 | CCMD-IIR | I: 32; C: 32 | I: 18–51; C: 19–56 | EA + Amitriptyline | EA: 1w-2w: 7 times/ w; 3w-6w: 3 times/ w; 6w; Amitriptyline: 1 time/ d, 50 mg/ time, 6 w | Amitriptyline | 2 times/ d, 25–75 mg/ time, 6 w | N/A | N/A | SDS(0, 3, 6w), SAS(0, 3, 6w); response rates |
Tian et al.62 | 2008 | 2 | CCMD-III | I: 30; C: 30 | I: 35.1 ± 14.3; C: 34.8 ± 15.1 | EA + Clomipramine* | EA: 5 times/ w, 6 w; Clomipramine: 1 time/d , 25–75 mg/ time, 6 w* | Clomipramine* | 1 time/d , 25–250 mg/ time, 6w; | N/A | N/A | HAMD-17(0, 6 w); response rates |
Wang et al.63 | 2018 | 2 | CCMD-III | I: 40; C: 40 | I: 34.2 ± 10.9; C: 33.4 ± 11.8 | MA + Fluvoxamine | 5 times/ w, 6w; Fluvoxamine: 100 ~ 150 mg/ d, 6 w | Fluvoxamine | 100 ~ 150 mg/ d, 6 w | N/A | N/A | HAMD-24(0, 2, 4, 6w), SERS(1, 2, 4, 6w); response rates |
Wang et al.64 | 2014 | 3 | ICD-10 | I: 23; C: 32; T:17 | I: 47 ± 11; C: 45 ± 12; T: 48 ± 9 | EA + Paroxetine | EA: 1 time/ 2 d, 6 w; Paroxetine: 10–20 mg/ d, 1 time/ d, 6 w | MA + Paroxetine | MA: 3 times/w, 6 w; Paroxetine: 10–20 mg/ d, 1 time/ d, 6 w | Paroxetine | 10–20 mg/ d, 1 time/ d, 6 w | HAMD-17(0, 1, 2, 4, 6w), SERS(0, 2, 4, 6w), WHOQOL—BREF(0, 6w); response rates |
Wang et al.65 | 2016 | 2 | DSM-IV | I: 32; C: 32 | I:41.3 ± 5.2;C:42.1 ± 4.7 | MA | 1 time/ d, 6 time/ w, 8 w | Mirtazapine | 1 time/ d, 15–45 mg/ time, 8 w | N/A | N/A | HAMD-24(0, 4, 8w); Asberg; response rates |
Wang et al.66 | 2007 | 3 | CCMD-III | I: 35; C: 35 | I: 17–65; C: 19–63 | EA | 5 times/ w, 12 w | Sertraline | 25–75 mg/ d, 12 w | HC | HC | HAMD-17(0, 2, 4, 8, 12) |
Wang et al.67 | 2007 | 2 | CCMD-III | I: 30; C: 30 | I: 18–68; C: 17–70 | EA* | 5 times/ w, 12 w* | Sertraline* | 25–7 5 mg/ d, 1 time/ d, 12 w* | N/A | N/A | HAMD-17(0, 2, 4, 8, 12) |
Wang et al.68 | 2006 | 2 | CCMD-III | I: 38; C: 38 | I: 18–65; C: 19–63 | EA* | 5 times/ w, 24 w* | Sertraline* | 25–75 mg/d, 1 time/ d, 24 w* | N/A | N/A | HAMD-17(0, 6, 12, 24); response rates |
Wang et al.69 | 2007 | 2 | CCMD-III | I: 50; C: 50 | I: 17–80; C: 19–73 | EA* | 5 time/ w, 12 w* | Sertraline* | 1time/ d, 25–75 mg/ time, 12 w* | N/A | N/A | HAMD-17(0, 2, 4, 8, 12w); response rates |
Wang et al.70 | 2008 | 2 | CCMD-III | I: 50; C: 42 | I: 52.8 ± 14.1; C: 52.1 ± 15.4 | MA + SSRIs* | MA: 5 time/w, 4w; SSRIs* | SSRIs* | SSRIs* | N/A | N/A | HAMD-17, SDS(0, 1, 2, 4w ); response rates |
Wang et al.71 | 2010 | 2 | ICD-10 | I: 30; C: 30 | I: 35.7 ± 11.1 C: 41.2 ± 9.0 | EA + Fluoxetine | EA: 7 times/ w, 6 w; Fluoxetine: 20 mg/ d, 1 time/ d, 6 w | Fluoxetine | 20 mg/ d, 1 time/ d, 6 w | N/A | N/A | HAMD-17(0, 2, 4, 6w); response rates |
Wang et al.72 | 2014 | 2 | ICD-9 | I: 47; C: 29 | NR | MA + SSRIs/ SNRIs | MA: 5 times/ w, 6 w; Fluoxetine: 20 mg, 1 time/ d; or Paroxetine: 20 mg, 1 time/d; r Duloxetine: 40 mg, 1 time/ d, 6w | SSRIs/ SNRIs | Fluoxetine: 20 mg, 1 time/ d; or Paroxetine: 20 mg, 1 time/d; r Duloxetine: 40 mg, 1 time/ d, 6w | N/A | N/A | HAMD-17 (0, 1, 2, 4, 6 w) |
Wang et al.73 | 2017 | 2 | ICD-10 | I: 22; C: 24 | I: 44.5 ± 10.47; C: 43.78 ± 9.10 | MA + Fluoxetine | MA : 1 time/d for the first three days, 1 time/ 3 d for the reminder of the 8-w trial; Fluoxetine: 20 mg/ d | Sham MA + Fluoxetine | Sham MA : 1 time/d for the first three days, 1 time/ 3 d for the reminder of the 8-w trial; Fluoxetine: 20 mg/ d | N/A | N/A | MADRS, SDS(0, 8 w) |
Wang et al74 | 2020 | 2 | CCMD-3 | I: 48; C: 48 | I: 34.19 ± 8.4; C: 32.71 ± 8.2 | Venlafaxine + MA* | MA: 3 times/ w, 12 w; Venlafaxine: 1st w:75 mg/d, 2ed w:150 mg/d, 3-6th w 225 mg/d, 12w* | Venlafaxine* | MA: 3 times/ w, 12 w; Venlafaxine: 1st w:75 mg/d, 2ed w:150 mg/d, 3-6th w 225 mg/d, 12w* | N/A | N/A | HAMD-17, SERS(0, 4, 8, 12 w); response rates |
Wang et al75 | 2019 | 3 | DSM-V | I: 30; C: 30; T:30 | I: 32 ± 8; C: 32 ± 7;32 ± 8 | Venlafaxine + MA* | MA: 3 times/ w, 12 w; Venlafaxine:1st w:75 mg/d, 2ed w:150 mg/d, 3-6th w 225 mg/d, 12w* | Venlafaxine * | 1st w:75 mg/d, 2ed w:150 mg/d, 3-6th w 225 mg/d, 12w* | HC | HC | HAMD-17, BDI(0,2,8,12w), SERS(2,8,12w) |
Wang et al.76 | 2013 | 2 | DSM-IV | I: 30; C: 30 | I: 48.1 ± 13.40; C: 47.10 ± 10.60 | EA | 3 times/ w, 24 w | Paroxetine | 20–60 mg/ d, 1 time/ d, 24 w | N/A | N/A | MMPI, MADRS, SDS, SAS(0, 24w) |
Wen et al.77 | 2003 | 2 | CCMD-III | I: 31; C: 30 | I: 31.6 ± 13.6; C:32.7 ± 14.1 | EA + SSRIs | EA: 1 time/ d, 6 w; SSRI | SSRIs | SSRIs | N/A | N/A | HAMD(0, 2, 4, 6w); response rates |
Wu et al.78 | 2010 | 2 | CCMD-III | I: 33; C: 33 | I: 68.52 ± 4.84; C: 69.64 ± 5.19 | EA + Citalopram | EA: 5 times/ w, 6w; Citalopram: 20–40 mg/ d, 6 w | Citalopram | 20–40 mg/ d, 6w | N/A | N/A | HAMD-17, TESS (0, 1, 2, 4, 6 w); response rates |
Xu et al.79 | 2009 | 2 | CCMD-III | I: 21; C: 20 | I: 34; C: 31 | MA | 6 w | Fluoxetine | 20 mg/d, 6 w | N/A | N/A | HAMD-17(0, 6 w); response rates |
Xu et al.80 | 2004 | 2 | CCMD-III、ICD-10 | I: 30; C: 30 | I: 42.5 ± 8.5; C:45.3 ± 9.2 | MA | 1 time/ d, 30d | Fluoxetine | 20–40 mg/ d, 1 time/ d, 30d | N/A | N/A | HAMD-24(0, 1, 2, 4w) |
Xu et al.81 | 2011 | 3 | CCMD-III | I: 25; C: 30; T: 25 | I: 47.51 ± 8.21; C: 47.42 ± 8.89; T: 48.01 ± 8.14 | MA + SSRIs | MA: 3 times/ w, 6 w; Paroxetine, 20–60 mg, 1 time/ d, 6 w; or Sertraline: 50–200 mg, 1 time/ d, 6 w; or Fluoxetine: 20–80 mg, 1 time/ d, 6 w | SSRIs | Paroxetine,20–60 mg, 1 time/ d, 6 w; or Sertraline: 50–200 mg, 1 time/ d, 6 w; or Fluoxetine: 20–80 mg, 1 time/ d, 6 w | MA + Moxibustion + SSRIs | MA + Moxibustion: 3 times/ w, 6 w; Paroxetine,20–60 mg, 1 time/ d, 6 w; or Sertraline: 50–200 mg, 1 time/ d, 6 w; or Fluoxetine: 20–80 mg, 1 time/ d, 6 w | HAMD-17(0, 1, 2, 4, 6w); response rates |
Yang et al.82 | 2012 | 3 | CCMD-III | I: 30; C: 30; T: 30 | I: 32.23 ± 13.98; C:33.40 ± 15.51; T:34.63 ± 12.71 | EA + CBT | 2 time/ w, 8 w; CBT: 1 time/w, 60-90 min/ time, 8 times | EA | 2 time/ w, 8 w | CBT | 1 time/w, 60-90 min/ time, 8 times | HAMD-17, CES-D(0.8w); response rates |
Yi et al.83 | 2011 | 3 | DSM-IV | I: 14; C:14; T:14 | I: 37.0 ± 8.6; C:33.6 ± 8.4; T:35.5 ± 7.4 | MA + Fluoxetine | MA: 5 time/w, 30 d; Fluoxetine: 1time/ d, 20 mg/ time, 30 d | Fluoxetine | 1 time/ d, 20 mg/ time, 30 d | MA | 5 time/ w, 30 d | HAMD-17(0, 30d) |
Zhang et al.84 | 2007 | 2 | CCMD-III | I: 38; C: 42 | I: 41.57 ± 1.22; C: 39.82 ± 2.16 | EA | 1 time/ d, 6 w | Paroxetine | 1 time/ d, 20 mg/ time, 6 w | N/A | N/A | HAMD-17(0, 2, 4, 6w) |
Zhang et al.85 | 2012 | 2 | CCMD-III | I: 20; C: 20 | I: 47.58 ± 9.45; C: 45.65 ± 10.45 | MA | 4 w | Flupentixol + Melitracen | Flupentixol: 0.5 mg/time + Melitracen: 10 mg/time; 1 time/ d, 4 w | N/A | N/A | HAMD-17(0, 4w); response rates |
Zhang et al.86 | 2007 | 2 | DSM-III | I: 22; C: 20 | I: 36.6 ± 9.7; C: 37.1 ± 10.2 | EA + Paroxetine | EA: 6 times/ w, 6 w; Paroxetine: 10–40 mg/ d, 6 w | Paroxetine | 10–40 mg/ d, 6 w | N/A | N/A | HAMD-17(0, 1, 2, 4, 6 w), TESS (1, 2, 4, 6 w); response rates |
Zhang et al.87 | 2009 | 2 | DSM-IV | I: 40; C: 40 | I: 36.2 ± 11.7; C: 35.5 ± 12.0 | MA + Fluoxetine (low dose) + placebo* | MA: 5 times/ w, 6 w; 10 mg fluoxetine + 1 placebo pill/ d in the first 2 w, followed by 10 mg fluoxetine + 2 placebo pills/d in the next 4 w* | Sham MA + Fluoxetine (normal dose)* | Sham MA: 5 times/ w, 6 w ; 20 mg/d in the first 2 w, followed by 30 mg fluoxetine/d in the next 4 w* | N/A | N/A | response rate, HRSD-17, HRSA (0, 2, 4, 6 w); SERS, acupuncture-specific side-effect checklist (2, 4, 6 w) |
Zhao et al.88 | 2010 | 3 | CCMD-III、DSM-IV | I: 30; C: 30; T: 30 | I: 36.5 ± 14.7; C: 39.1 ± 12.3; T: 37.1 ± 12.3 | EA | 1 time/ d, 5 time/ w, 6w | EA | 1 time/ d, 5 times/ d, 6 w | Fluoxetine | 20 mg/ time, 1 time/ d, 6 w | HAMD-24(0, 2, 4, 6 w); response rates |
Zhao et al.89 | 2010 | 2 | CCMD-III | I: 48; C: 45 | I: 40.9 ± 13.9; C: 41.5 ± 13.9 | EA + Paroxetine* | EA: 7 times/ w, 3 w; Paroxetine: 10–40 mg/ d, 3 w* | Paroxetine* | 10–40 mg/ d, 3 w* | N/A | N/A | HAMD(0, 3w); response rates |
Zhao et al.90 | 2006 | 2 | CCMD-III | I: 38; C:38 | I: 18–65; C:19–63 | EA* | 5 time/ w, 12 w* | Sertraline* | 1 time/ d, 25–75 mg/ time, 12 w* | N/A | N/A | HAMD-17(0, 1, 2, 8); response rates |
Zhao et al.91 | 2019 | 3 | ICD-10 | I: 161; C: 160; T:156 | I: 41.42 ± 12.53;C: 41.18 ± 12.00; T: 41.76 ± 12.85 | MA + SSRIs | MA: 3 times/ w, 6 w; Paroxetine, Fluoxetine, Sertraline, Fluvoxamine, Citalopram, or Escitalopram: 10–20 mg/d, 6 w | EA + SSRIs | EA: 3 times/ w, 6 w; Paroxetine, Fluoxetine, Sertraline, Fluvoxamine, Citalopram, or Escitalopram :10–20 mg/d, 6 w | SSRIs | Paroxetine, Fluoxetine, Sertraline, Fluvoxamine, Citalopram, or Escitalopram: 10–20 mg/d, 6 w | response rate, remission rate(6w); early onset rate(1w), HAMD-17(0,1,2,4,6,10w), SDS(0,1,2,4,6,10w), CGI(6w), SERS(2,4,6w) |
Zheng et al.92 | 2012 | 2 | CCMD-III | I: 44; C: 54 | I: 47.11 ± 9.52; C: 48.07 ± 10.09 | MA | 1 time/ 2d, 3 times/ w, 6 w | SSRI | Paroxetine,20–60 mg, 1 time/ d, 6 w; or Sertraline: 50–200 mg, 1 time/ d, 6 w; or Fluoxetine: 20–80 mg, 1 time/ d, 6 w | N/A | N/A | HAMD-17(0, 1, 2, 4, 6w, f), SERS(0, 1, 2, 4, 6w); response rates |
Zhu et al.93 | 2018 | 2 | CCMD-III | I: 33; C: 32 | I: 42.9 ± 5.0; C:42.1 ± 4.3 | MA + SSRIs* | MA: 5 time/ w, 6w; SSRIs, 6w* | SSRIs* | SSRIs, 6w* | N/A | N/A | HAMD-24,heart rate variability (0, 6w) |