Andersson 2003.
Methods | Randomised clinical trial. | |
Participants | Country: Sweden.
Number randomised: 20.
Mean age: 39 years.
Females: 14 (70%). Inclusion criteria:
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Interventions | Participants were randomly assigned to two groups: Group 1: abdominal wall lift (n = 10). Group 2: pneumoperitoneum with 11 to 13 mm Hg pressure (n = 10). Device used for abdominal lift: intra‐peritoneal device. |
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Outcomes | The outcome measure was operating time. | |
Notes | One cross‐over participant from abdominal wall lift group to control due to poor visualisation. Attempts were made to contact the author in February 2007. |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Comment: This information was not available. |
Allocation concealment (selection bias) | Unclear risk | Comment: This information was not available. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Comment: This information was not available. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Comment: This information was not available. |
Incomplete outcome data (attrition bias) All outcomes | High risk | Comment: There were post‐randomisation drop‐outs. |
Selective reporting (reporting bias) | High risk | Comment: Important outcomes were not reported. |
Vested interest bias | Unclear risk | Quote: "This study was supported by Karolinska Institute." Comment: Not clear whether this was the only source of support. |