Methods |
RCT, multi‐centre study (6 centres) |
Participants |
101 participants (101 IVF/ICSI cycles) analysed |
Interventions |
COH included recombinant FSH (recFSH; Puregon) in flexible multi‐dose GnRH antagonist protocol (orgalutran). Triggering was randomly performed by 10,000 IU HCG (Pregnyl) or 0.1 mg GnRH agonist (triptorelin) |
Outcomes |
Serum concentrations of LH, FSH, E2 and P4 were measured at 0, 12, 36 and 108 hours after triggering |
Notes |
|
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Unclear risk |
Insufficient information: Full text was unavailable |
Allocation concealment (selection bias) |
Unclear risk |
Insufficient information: Full text was unavailable |
Blinding (performance bias and detection bias)
FOR OHSS OUTCOME |
Unclear risk |
Insufficient information: Full text was unavailable |
Incomplete outcome data (attrition bias)
All outcomes |
Unclear risk |
Insufficient information: Full text was unavailable |
Selective reporting (reporting bias) |
Unclear risk |
Insufficient information: Full text was unavailable |
Other bias |
Unclear risk |
Insufficient information: Full text was unavailable |