Clinical Trials · NCT01110707
A Randomised, Phase II, Comparative Study With a Parallel Control for Evaluating the Efficacy and Safety of Combined Treatment of Lutropin Alpha and Recombinant Human Luteinizing Hormone in the Middle of the Controlled Ovarian Stimulation Follicular Phase in Women With Reduced Ovarian Reserve
- Phase
- Phase 2
- Recruitment status
- Completed
- Sponsor
- Merck KGaA, Darmstadt, Germany
- Enrollment
- 131
- Start date
- Jan 2005
- Locations
- 1 site, Spain
- Primary endpoint
- Mean Number of Metaphase II (M-II) Oocytes Retrieved