drugset / Trial / NCT00329693

Study Assessing the Effect of 3-week Treatment With One of Three Oral Doses of Quinagolide

NCT00329693

Phase 2 Completed 182 enrolled Ferring Pharmaceuticals
RandomizedParallel-groupDouble-blindPrevention

Summary

Women included in this study are undergoing controlled ovarian hyperstimulation for assisted reproductive technologies (ART) and present with signs of moderate risk of developing OHSS.

Timeline

Start
2006-06
Primary completion
2007-08
Completion
2008-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Quinagolide Other / unclassified 50 ug Oral
Subject Quinagolide Other / unclassified 100 ug Oral
Subject Quinagolide Other / unclassified 200 ug Oral