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Comparison of Different Methods for Luteal Phase Support in IVF / ICSI Cycles With Antagonist Protocol in Women With Poor Ovarian Response
This study is a randomized clinical trial to investigate the efficacy of different luteal phase support methods in patients with poor ovarian response undergoing IVF and intracytoplasmic sperm injection (ICSI) cycles. The study protocol is approved by the Ethics Committee (Institutional Review Board) of Royan institute. The study is conducted according to the Declaration of Helsinki for medical research. All participants provide informed consent after counseling for infertility treatments and routine IVF/ICSI programs.
Details
| Lead sponsor | Royan Institute |
|---|---|
| Phase | Phase 3 |
| Status | UNKNOWN |
| Enrolment | 210 |
| Start date | 2015-11 |
| Completion | 2019-12 |
Conditions
- Infertility
Interventions
- Choriomon® injection
- Choriomon® injection+Endometrin ®
- Endometrin ® vaginal tablets
Primary outcomes
- Clinical pregnancy rate — 4 weeks
Evaluation the clinical pregnancy rate at least 4 weeks after embryo transfer.
Countries
Iran