Khattar 2007.
Study characteristics | ||
Methods | This study was carried out in a secondary care setting. This study was blinded. Intention‐to‐treat analysis was carried out. This study was conducted in the USA. |
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Participants | 44 participants were recruited: None dropped out. Inclusion criteria of the trial
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Interventions |
These were applied twice daily, over 3 months. |
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Outcomes |
Outcomes of the trial
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Notes | The number of warts per participant ranged from 1 to 41, and the study was aiming for cure of all warts in each participant. There was a higher mean number of warts in the zinc oxide group (5.1 versus 4.3), and participant compliance was not assessed. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote (page 427): "Patients were assigned randomly to two groups." Comment: The method of randomisation was unclear. |
Allocation concealment (selection bias) | Unclear risk | The allocation concealment was unclear. |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | The medication was labelled A or B; therefore, participants were unaware which treatment they were receiving. Personnel were blinded. Quote (page 427): "At the end of the study the pharmacist informed the primary investigator that arm A was 20% zinc oxide and arm B was the 15% alicyclic acid." Comment: This was probably done for both participants and personnel. |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | It was not specifically stated that outcome assessors were blinded. Comment: This was judged as probably done as the personnel were blinded. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | 9/44 participants withdrew: 6/22 in the zinc oxide group and 3/22 in the SA‐LA group. Reasons were not stated. There be may be a source of bias arising from 1 participant with 41 warts who withdrew. |
Selective reporting (reporting bias) | Low risk | All outcomes were reported. |