Macdermid 2003.
Methods | Single centre RCT | |
Participants | Participants were randomised in an unbalanced design with a 3:1 probability of receiving an endoscopic procedure (91 ECTR, 32 OCTR). Age 45 ± 15 for ECTR and 53 ± 16 for OCTR. Women comprised 68% of both arms (demographics were similar between groups) CTS confirmed by electrophysiology, and participants had poor response to 6 months' conservative treatment |
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Interventions | 2‐portal ECTR (transbursal ‐ Chow technique) vs OCTR | |
Outcomes | Follow‐up at 1 and 6 weeks and 3 months SSS, serious complications, grip strength, pinch strength, sensory threshold, pain (McGill pain questionnaire), time to return to work, rate of repeat procedures (at > 2 years follow‐up) |
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | No information given in the manuscript |
Allocation concealment (selection bias) | Unclear risk | No information given in the manuscript |
Blinding of participants and personnel (performance bias) All outcomes | High risk | No information given. Participants and personnel could not be blinded |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | The authors state that "all evaluations were performed by a blinded evaluator" , although there was no additional information given regarding the way of blinding (eg gloves used) |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | No information given in the manuscript regarding potentially losses to follow‐up and how they were addressed |
Selective reporting (reporting bias) | Unclear risk | The authors only provide diagrams, with no SDs or P values |
Other bias | Unclear risk | Groups were similar at baseline but only in demographics. No statistical analysis was provided regarding measurements at baseline, although such measurements had been conducted The authors declare no conflict of interest or financial support |