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NCT05838105

Two Different Types of Luteal Phase Support in Natural Cycle Frozen Embryo Transfer and Its Effect on Pregnancy Rates

Status unknown NA Last updated 1 May 2023
What this trial tests

NA trial testing GnRH agonist in Luteal Phase Support in 144 participants. Status unknown.

Timeline
1 October 2022
Primary endpoint
1 January 2025
1 January 2025

Quick facts

Lead sponsorShaare Zedek Medical Center
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment144
Start date1 October 2022
Primary completion1 January 2025
Estimated completion1 January 2025
Sites1 location across Israel

Drugs / interventions tested

Conditions studied

Sponsor

Shaare Zedek Medical Center

Who can join

Adults 18 to 45, female only, with Luteal Phase Support. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to compare the pregnancy rate between women treated with Gonadotropin Releasing Hormone (GnRH) agonist together with Human Chorionic Gonadotropin (HCG) and standard luteal support with progesterone following transfer of frozen embryos in in-vitro-fertilization (IVF) natural cycles.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of GnRH agonist

Trials testing the same drug.

Other recruiting trials for Luteal Phase Support

Currently open trials in the same condition.

Other Shaare Zedek Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05838105.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing