Banihashemi 2008.
Study characteristics | ||
Methods | This study was carried out in a secondary care setting. This study was blinded. Intention‐to‐treat analysis was not carried out. This study was conducted in Singapore. |
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Participants | 60 participants were recruited: 7 dropped out. The average age of the participant was 15.6 years in the intervention group and 16.4 years in the control group. Inclusion criteria of the trial
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Interventions |
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Outcomes |
Outcomes of the trial
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Notes | ‐ | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote (page 1035): "Patients were randomly divided into two groups." Comment: The method used was simple randomisation according to the method of Lachin 1981 (additional information came from the trial investigator). |
Allocation concealment (selection bias) | Unclear risk | The allocation concealment was unclear; no information was given. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | The trial investigators said: "Patients and the first dermatologist who treated them were alert about the medication." Comment: This was not blinded. |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Outcome assessors were blinded to the treatment (additional information came from the trial investigator). |
Incomplete outcome data (attrition bias) All outcomes | High risk | 7 cases in the phenol group were not followed up. Quote (page 1036): "Four did not complete the follow‐up period and three could not tolerate burning sensation." Comment: Uneven distribution across the groups was likely to introduce bias. |
Selective reporting (reporting bias) | Low risk | All prespecified outcomes were reported. |