Abdel‐Aleem 2012.
Study characteristics | ||
Methods | RCT. | |
Participants | Inclusion criteria:
Exclusion criteria:
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Interventions | Intervention: corticosteroid (Comparison 3)
Comparator: placebo
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Outcomes | Nausea, vomiting, number of vomiting attacks, need for anti‐emetics, sedation, itch, respiratory depression, pain, satisfaction (retching classified as vomiting). | |
Notes | Setting: Assiut University Hospital, Egypt. Dates: February 2008 to December 2009. Funding source: not reported Declaration of interest: none declared. We wrote to authors for clarification on whether the 53 women were excluded pre or post randomisation as it is unclear from the text of the publication. Spinal with bupivacaine and 200 mcg IT morphine |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: "computer based random allocation table" |
Allocation concealment (selection bias) | Low risk | Quote:“sealed opaque envelopes consecutively numbered and coded” |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | the patient ... was unaware of which intervention had been received |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Those assessing the outcomes were also unaware of which intervention had been received. |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | 53 patients were excluded enrolment although it is unclear if this was before or after randomisation. |
Selective reporting (reporting bias) | Unclear risk | We were unable to assess the trial protocol. |
Other bias | Low risk | Similar baseline characteristics |