drugset / Trial / NCT00827983

Subcutaneous Progesterone Versus Vaginal Progesterone Gel for Luteal Phase Support in Patients Undergoing In-Vitro Fertilization (IVF)

NCT00827983

Phase 3 Completed 683 enrolled IBSA Institut Biochimique SA
RandomizedParallel-groupOpen-labelTreatment

Summary

Prospective, open, randomised, parallel, multicentre, two arm trial comparing a new form of luteal support (S.C.) to an approved comparator (vaginal gel).

Timeline

Start
2009-01
Primary completion
2010-11
Completion
2011-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator Progesterone Other / unclassified 25 mg Subcutaneous
Comparator Progesterone Other / unclassified 90 mg Subcutaneous

Indications

No indication recorded.