WHO ICTRP trial

Rectally administered micronized progesterone for luteal phase support in…

CTIS2023-504616-15-02 · EU Clinical Trials Information System · Not Recruiting

Key facts

Trial ID CTIS2023-504616-15-02
Public title Rectally administered micronized progesterone for luteal phase support in hormone replacement therapy frozen embryo transfer (HRT-FET) cycle – non-inferiority randomized controlled trial
Scientific title Rectally administered micronized progesterone for luteal phase support in hormone replacement therapy frozen embryo transfer (HRT-FET) cycle – non-inferiority randomized controlled trial
Primary sponsor Fertiltetsklinikken, Regionshospitalet Skive
Registry EU Clinical Trials Information System
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use - (Phase IV): no
Countries Denmark
Conditions Infertility;Therapeutic area: Diseases [C] - Female Urogenital Diseases and Pregnancy Complications [C13]
Interventions Product Name: Cyclogest 400mg,Product Code: PRD6391564,Pharmaceutical Form: PESSARY,Other descriptive name: ,Strength: Progesterone Ph. Eur. 400mg,Product Name: Estrofem 2 mg Filmtabletten,Product Code: PRD1608213,Pharmaceutical Form…
Registration date Nov 9, 2023
Target size 618
Registry page euclinicaltrials.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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