At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Lutropin Alfa (Luveris®) in Women at Risk of Poor Response Suppressed With Cetrorelix: an Exploratory Trial
In Brief
A Phase 2 clinical trial evaluating r-FSH, r-hLH, and 3 other interventions for Ovarian Stimulation. Completed, enrolled 58 participants across 1 site.
Detailed Summary
Evaluate the effectiveness of adding lutropin alfa (recombinant human luteinizing hormone \[r-hLH\]) in the middle of the follicular phase compared to no addition, in infertile women at risk of poor response stimulated with follitropin alfa (recombinant Follicle-Stimulating Hormone \[r-FSH\]) under Gonadotropin Releasing Hormone (GnRH) antagonist in vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI), in the number and quality of oocytes, follicular development, fertilization oocyte, embryo quality, and pregnancy rate.
Study Details
Timeline
Interventions
r-FSH will be administered as specified in the arm description.
r-hLH will be administered as specified in the arm description.
Analogous GnRH antagonist will be administered as specified in the arm description.
r-hCG will be administered as specified in the arm description.
Progesterone will be administered as specified in the arm description.