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RECRUITING
NCT04725864
PHASE4

Progesterone as Luteal Support in Frozen IVF Natural Cycles

Sponsor: Vastra Gotaland Region

View on ClinicalTrials.gov

Summary

The ProFET study aims to investigate if luteal phase support by vaginal progesterone, is superior to no luteal phase support, in terms of live birth rate per woman after a frozen embryo transfer (FET), in a natural cycle (NC) after in-vitro fertilization (IVF), and if 7 weeks of treatment is superior to 3 weeks duration.

Official title: Vaginal Progesterone as Luteal Support for Improvement of Live Birth in Frozen/Thawed In-vitro Fertilization Natural Cycles; a Multicenter, Open, Randomized Trial

Key Details

Gender

FEMALE

Age Range

18 Years - 43 Years

Study Type

INTERVENTIONAL

Enrollment

1800

Start Date

2021-05-01

Completion Date

2025-12-31

Last Updated

2024-04-24

Healthy Volunteers

No

Interventions

DRUG

Progesterone vaginal tablet

The study drug is progesterone 100 mg administrated as a vaginal tablet three times daily.

Locations (1)

Department of Reproductive Medicine

Gothenburg, Sweden