Seropian 1971.
Study characteristics | ||
Methods | QRCT | |
Participants | 406 people undergoing surgery, excluding endoscopy, fractures, burns, oral surgery, abscesses, proctological and vaginal surgery, in the USA between June 1968 and February 1969 | |
Interventions | Group 1: hair removal with a razor (n = 249)
Group 2: hair removal with depilatory cream (n = 157) Product details: no details are given for the razor, the cream consisted of calcium thioglycollate, calcium hydroxide, and strontium hydroxide. Timing of hair removal: not reported. Hair removed by: not reported. Venue for hair removal: not reported. |
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Outcomes | Outcome: evidence of wound infection as recorded by wound infection control office through case follow‐up and weekly review; no further details given. | |
Notes | The study was supported by a grant from CIBA Pharmaceutical Company. No details of conflict of interest. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | High risk | Quote: the method used was "determined arbitrarily by the last digit of the patient's hospital number". Comment: non‐random approach. |
Allocation concealment (selection bias) | High risk | Quote: the method used was "determined arbitrarily by the last digit of the patient's hospital number". Comment: the person allocating participants to groups would have been able to predict to which group a potential participant would be allocated. |
Blinding (performance bias and detection bias) Care providers blinded | Unclear risk | Not reported. Comment: unclear whether care providers were blinded to intervention allocation. |
Blinding (performance bias and detection bias) Participants blinded | High risk | Not reported. Comment: participants would have been aware of hair removal method. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not reported. Comment: unclear whether assessors were blinded to intervention allocation. |
Incomplete outcome data (attrition bias) ITT analysis undertaken | Unclear risk | Not reported. Comment: no discussion of whether participants were analysed in the groups to which they had been allocated. |
Incomplete outcome data (attrition bias) Drop out rate acceptable | High risk | Reasons for dropouts were given, but group sizes appeared to be unequal. Comment: participants were not evenly distributed across groups. |
Selective reporting (reporting bias) | Low risk | Main outcomes reported. Comment: unlikely to be affected by reporting bias. |
Other bias | Low risk | Comment: participant groups were equal or similar. |