Post-Marketing Surveillance of the Safety and Efficacy of Orgalutran (Ganirelix)®

NCT01304511 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 711

Last updated 2024-04-03

No results posted yet for this study

Summary

The purpose of this post-marketing surveillance is to identify problems and questions regarding the safety and efficacy of Orgalutran (Ganirelix)® when used for the prevention of premature luteinizing hormone (LH) surges in women undergoing controlled ovarian hyperstimulation (COH) for assisted reproduction techniques (ART).

Conditions

  • Fertilization in Vitro

Interventions

DRUG

Orgalutran

Sponsors & Collaborators

  • Organon and Co

    lead INDUSTRY

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-02-28
Primary Completion
2007-12-31
Completion
2007-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01304511 on ClinicalTrials.gov