Luteal Phase Defect Clinical Trial
Official title:
Progesterone Levels and Clinical Outcomes Using a Single Pessary of 400 mg of Vaginal Progesterone in Substitutive Cycles for Embryo Transfer.
This study aims to compare the efficacy, in terms of progesterone levels and clinical outcomes, of two different presentations of micronized vaginal progesterone (400 mg vs. 200 mg) used in endometrial preparation in artificial cycle (AC) for embryo transfer. This is a non-inferiority, retrospective case-control study, with at least 200 cycles analyzed (at least 100 per arm) and the primary outcome is the serum progesterone level on the day of the embryo transfer.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01178931 -
Dydrogesterone Versus Intravaginal Progesterone in the Luteal Phase Support
|
N/A | |
Completed |
NCT04174378 -
Luteal Phase Support In IVF Women Using GnRH Agonist
|
||
Withdrawn |
NCT02950948 -
Progesterone in Luteal Phase Deficiency
|
Phase 3 | |
Completed |
NCT04938622 -
Bioenergetics of Exercise-Induced Menstrual Disturbances
|
N/A | |
Completed |
NCT02458404 -
Effects of Varied Estrogen Doses on Endometrial Receptivity
|
||
Completed |
NCT05107804 -
Energy Restriction and Hormones in Premenopausal Women
|
N/A | |
Completed |
NCT03948022 -
Luteal Support in Frozen-Thawed Embryo Transfer Cycles
|
Phase 4 | |
Not yet recruiting |
NCT05080569 -
Luteal Phase Support in IUI MOH Treatment Luteal Phase Support in IUI MOH Treatment
|
Phase 4 | |
Recruiting |
NCT04806919 -
Luteal Support in Artificial Vitrified/Warmed Cycles With Low Progesterone
|
Phase 3 |