Fredriksson 1978.
Methods | Parallel‐arm randomised controlled trial Number of centres not stated Period of inclusion not stated |
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Participants |
Inclusion criteria Not stated Exclusion criteria Not stated Baseline data: randomised to RO 10‐9359 (25 mg thrice per day) (n = 15) or RO 10‐9359 (200 mg twice per week) (n = 15)
Withdrawal: no mention of missing data |
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Interventions |
Intervention 1 A: oral RO 10‐9359 (25 mg thrice per day) (15 participants) Intervention 2 B: oral RO 10‐9359 (200 mg twice per week) (15 participants) Co‐interventions: none Duration of treatment: 8 weeks |
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Outcomes | No primary or secondary outcomes pre‐specified
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Notes | Funding: not reported | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote: "30 patients randomly allocated to two treatment groups" Comment: insufficient information about the sequence generation process to permit judgement |
Allocation concealment (selection bias) | Unclear risk | Quote: "30 patients randomly allocated to two treatment groups (one group treated with etretinate 75 mg daily and the other with 200 mg twice weekly)" Comment: the method to guarantee allocation concealment is not described |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Comment: no mention of blinding |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Comment: no mention of blinding |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Comment: no mention of missing data |
Selective reporting (reporting bias) | Unclear risk | Comment: no protocol found to guarantee that all planned outcomes are presented in the results |