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Phase 4 Completed N=384 Randomized Treatment

Triggering of Final Oocyte Maturation With GnRHa (Buserelin) in GnRH Antagonist Cycles

OHSS (Ovarian Hyperstimulation)
Source: ClinicalTrials.gov NCT00627406 ↗
Enrolled (actual)
384
Serious AEs
0.0%
Results posted
Nov 2013
Primary outcomePrimary: Frequency of Moderate to Severe OHSS. — 0; 2; 2; 0 participants

Summary

The purpose of this study is to possibly further improve the clinical outcome and explore the incidence of OHSS in patients, who have final oocyte maturation with GnRHa (Buserelin) in GnRH antagonist IVF/ICSI cycles

Outcome Measures

OutcomeResultp-value
PRIMARY
Frequency of Moderate to Severe OHSS.
0; 2; 2; 0
SECONDARY
Pregnancy Rate
17; 15; 37; 36

Eligibility Criteria

Inclusion Criteria

  • Patient complying with the conditions for IVF or ICSI treatment
  • Female age over 20 years and under 40 years
  • Normal regular cycle and patients with oligomenorrhea
  • BMI > 18 and 25 follicles on the day of triggering ovulation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00627406). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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