Apt 1998*.
Methods | Non‐randomised study | |
Participants | Adults | |
Interventions | ALLOP (n = 104) 8.5 mg/kg/day (8 weeks) ITRA (n = 135) 6 mg/kg/day (16 weeks) Placebo (n = 165) |
|
Outcomes | Xenodiagnosis recorded Side effects |
|
Notes | Chile 1998 | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Unclear |
Allocation concealment (selection bias) | Unclear risk | Unclear |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | |
Incomplete outcome data (attrition bias) All outcomes | Low risk |