Egawa 2006.
Methods | Randomised clinical trial. | |
Participants | Country: Japan.
Number randomised: 30.
Mean age: 50 years.
Females: 14 (46.7%). Inclusion criteria:
Exclusion criteria: Pre‐existing cardiovascular, respiratory or cerebrovascular disease. |
|
Interventions | Participants were randomly assigned to two groups: Group 1: abdominal wall lift (n = 15). Group 2: pneumoperitoneum with 10 to 12 mm Hg pressure (n = 15). Device used for abdominal lift: not stated. |
|
Outcomes | The outcome measure reported was operating time. | |
Notes | Attempts were made to contact the author in February 2007. | |
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. |