Rein 1996.
Methods | Randomised controlled trial | |
Participants | Women undergoing IVF cycles; 25 women participated, 34 cycles | |
Interventions | 0.5 of dexamethasone versus placebo | |
Outcomes | number of follicles >12 mm in diameter serum oestradiol concentrations on the day of hCG administration number of ampoules of HMG administered number of oocytes retrieved percentage of oocytes fertilised number of embryos transferred implantation rate numbers of clinical pregnancies and live birth pregnancies |
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Notes | Data per cycle not per woman; no response to our requests for per woman data. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | "The randomization scheme was based on computer‐generated permuted blocks ..." |
Allocation concealment (selection bias) | Low risk | "Compliance with the study medications was confirmed by our nurse coordinator" |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | "The clinical investigators and patients remained blinded to the treatment group throughout the duration of the study" |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | "The clinical investigators and patients remained blinded to the treatment group throughout the duration of the study" |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Could not get the necessary data from the trial author |
Selective reporting (reporting bias) | Unclear risk | Could not get the necessary information from the trial author |
Other bias | Unclear risk | Nine patients undergoing a subsequent IVF cycle were crossed over to the other treatment group (unclear how many from each group). |
ICSI: intra‐cytoplasmic sperm injection IVF: in‐vitro fertilisation hCG: human chorionic gonadotropin HMG: human menopausal gonadotropins OHSS: ovarian hyperstimulation syndrome PCOS: polycystic ovarian syndrome