Lindgren 1995.
Methods | Randomised clinical trial. | |
Participants | Country: Finland.
Number randomised: 25.
Mean age: 49 years.
Females: 22 (88%). Inclusion criteria:
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Interventions | Participants were randomly assigned to two groups: Group 1: abdominal wall lift with or without pneumoperitoneum (pressure not stated) (n = 12). Group 2: pneumoperitoneum with 12 to 15 mm Hg pressure (n = 13). Device used for abdominal lift: intra‐peritoneal device. |
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Outcomes | The main outcome measure was operating time. | |
Notes | Attempts were made to contact the author in February 2007 as besides missing data, a conference abstract publication with 24 patients was identified. Reading through the text, we could assume that the published conference abstract had presented data on the same trial. However the conference abstract did not report any outcomes of interest and the inclusion or exclusion of the abstract makes no difference to any of the effect estimates. | |
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 | Unclear risk | Comment: This information was not available. |
Selective reporting (reporting bias) | High risk | Comment: Important outcomes were not reported. |
Vested interest bias | Unclear risk | Comment: This information was not available. |