Murdoch 1991.
Methods | Trial design: parallel UK |
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Participants | Couples with unexplained subfertility N randomised: 39; IUI + NC 19; IUI + OH 20 Age: IUI + NC 30.5 years (± 3.1); IUI + OH 30.1 years (± 2.9) Duration of subfertility: IUI + NC 5.7 years (± 2.4); IUI + OH 5.1 years (± 1.9) Basic fertility work‐up done, semen normal (according to WHO 1987) Previous treatment: no |
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Interventions | Comparison: IUI + NC versus IUI + OH (vs GIFT)
Stimulation method: 75 IU hMG/day and 200 micro gram buserelin 4 times daily intranasal
Ovulation: 5000 IU hCG, when < 4 follicles of > 16mm were seen.
Timing: 30 hr to 36 hr after hCG
Natural cycle: IUI on alternate days until ovulation confirmed on USS
Cycles were cancelled if > 4 dominant follicles were present Duration of treatment: 3 cycles max |
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Outcomes | PR per couple and per cycle
Live birth
Multiple pregnancies Clinical pregnancy defined by USS showing foetal heart activity |
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Notes | ITT analysis: yes
Author provided additional information 1 pregnancy between treatment cycles 10 cycles were abandoned because no treatment available at the weekend |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer‐generated random‐number sequence |
Allocation concealment (selection bias) | Low risk | Adequate; sequentially numbered opaque sealed envelopes |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Blinding was not possible because of the nature of the interventions |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Blinding was not possible because of the nature of the interventions and non‐blinding was not likely to affect the outcomes of interest |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Drop‐out rate 3/19 (IUI + NC), and 2/20 (IUI + OH) |
Selective reporting (reporting bias) | Low risk | Live birth data were provided |
Other bias | Low risk | Nothing detected |