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. 2021 Sep 12;2021(9):CD011612. doi: 10.1002/14651858.CD011612.pub3

Ghasemi 2013.

Study characteristics
Methods Randomised controlled trial
Participants Diagnosis: DSM‐IV major depressive episode (1 bipolar disorder, depressed)
N: 18
Age: ketamine group M = 35.22 (SD = 13.63); ECT group M =40 (SD = 16.41)
Sex: ketamine group 56% female; ECT group 56% female
Baseline depression severity: ketamine group HRSD = 30.22 (SD = 5.78); ECT group HRSD = 35.88 (SD = 6.47)
Interventions 1 week of treatment
Ketamine (N = 9) 0.5 mg/kg over 45 minutes, 1 IV infusion every 48 hours
ECT (N = 9) 3 bilateral ECT sessions every 48 hours. During each ECT procedure, patients were administered 0.5 mg atropine followed by 2–3 mg/kg thiopental intravenously(IV); succinylcholine (0.5 mg/kg) was administered as a muscle relaxant after the induction of anaesthesia
Concomitant treatment: yes, patients continued existing treatments for depression
Outcomes BDI
HRSD
Response rates (≥ 50% reduction in HRSD scores)
Adverse events
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk No details given on randomisation procedure beyond ''randomly assigned''
Allocation concealment (selection bias) Unclear risk No details given on allocation concealment
Blinding of participants and personnel (performance bias)
All outcomes Low risk Quote: ''Treatment team members, including physicians and psychologists conducting the rating scales, were blinded to the treatment group except for the anesthesiologist''
Blinding of outcome assessment (detection bias)
All outcomes Low risk Quote: ''Treatment team members, including physicians and psychologists conducting the rating scales, were blinded to the treatment group except for the anesthesiologist''
Incomplete outcome data (attrition bias)
All outcomes Low risk Study reports dropouts (zero)
Selective reporting (reporting bias) Low risk Protocol unavailable, but means and SDs of all measures specified in methods section reported at all time points
Other bias Low risk No other potential sources of bias identified