Ali 2021.
| Study characteristics | ||
| Methods |
Design: parallel‐group RCT Study period: December 2017–December 2018 |
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| Participants |
Setting: elective general or colorectal surgery Type of stoma: ileostomy Inclusion criteria
Exclusion criteria
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| Interventions | PSSC using subcuticular absorbable suture (n = 37) versus LSC using interrupted non‐absorbable suture (n = 35). No mesh or drain was used during closure in either group. | |
| Outcomes |
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| Notes | The 2 groups were comparable in terms of baseline demographics (age, sex, BMI) and comorbidities. The length of follow‐up was 3 months. The study received no external funding, and the protocol had been registered with the Chinese Clinical Trial Registry (registration number: ChiCTR 1900025624). The study authors declared no conflicts of interest. | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | Article describes method of randomisation but not type of randomisation. |
| Allocation concealment (selection bias) | Low risk | The method used for randomisation supports allocation concealment. |
| Blinding of participants and personnel (performance bias) All outcomes | High risk | Participants and personnel were not blinded (blinding may not be practical in this setting). |
| Blinding of outcome assessment (detection bias) All outcomes | High risk | Outcome assessment was not blinded (blinding may not be practical in this setting). |
| Incomplete outcome data (attrition bias) All outcomes | Low risk | Complete outcome data for all participants. |
| Selective reporting (reporting bias) | Low risk | No selective reporting detected. |
| Other bias | Low risk | No other sources of bias detected. |