Methods |
RCT n=60 |
Participants |
CAF |
Interventions |
GTN 0.2% bid vs. diltiazem 2% bid 6 weeks |
Outcomes |
Healing
Pain relief
recurrence
Headache |
Notes |
ROK
ITT + |
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Low risk |
ROK |
Allocation concealment (selection bias) |
Low risk |
A ‐ Adequate |
Blinding (performance bias and detection bias)
All outcomes |
Low risk |
|
Selective reporting (reporting bias) |
Low risk |
appropriate outcomes/side effects reported |
Other bias |
Low risk |
ITT+ |
Blinding of participants and personnel (performance bias)
All outcomes |
Low risk |
|
Blinding of outcome assessment (detection bias)
All outcomes |
Low risk |
|
Duration of Follow‐up 6 months or more |
High risk |
12 weeks |