Progesterone as Luteal Support in Frozen IVF Natural Cycles

Infertility Clinical Trial

— ProFET  

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04725864
• Other study ID #: 2020-005552-38
• Status: Recruiting
• Phase: Phase 4
• Start date: May 1, 2021
• Est. completion date: December 31, 2025

Study information

• Verified date: April 2024
• Source: Vastra Gotaland Region
• Contact: Åsa Magnusson, MD, PhD
• Phone: +46 70-265 55 85
• Email: asa.magnusson[@]vgregion.se
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Description:

Vaginal progesterone supplementation is routine treatment after IVF with fresh embryo transfer, but it is uncertain whether vaginal progesterone after frozen embryo transfer in natural cycles is efficacious in terms of increasing the chance of a live birth.

The ProFET study is a multicenter, open randomized, controlled trial planning to include 1800 women, intended to undergo a FET in a natural cycle.

Primary objectives are 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, in a natural cycle and if 7 weeks of treatment is superior to 3 weeks duration.

Secondary objectives are to compare groups regarding pregnancy outcomes including biochemical pregnancy, clinical, ongoing and term pregnancy rates, as well as rates of miscarriage, termination of pregnancy, and ectopic pregnancy.

Secondary objectives are also perinatal and obstetrics outcomes, self-reported side effects, adverse events and cost effectiveness.

The investigators will also analyze the effect of S-Progesterone level before FET on the chance of achieving live birth and secondary pregnancy outcomes.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1800
• Est. completion date: December 31, 2025
• Est. primary completion date: June 30, 2025
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 43 Years

Eligibility

Inclusion Criteria:

• Planned for a FET-NC with a blastocyst

• BMI >18.5 <35

• Regular menstrual cycles 24-35 days

• Given informed consent

• Understand written and spoken Swedish, English or Arabic

Exclusion Criteria:

• Oocyte donor cycles, preimplantation genetic testing (PGT) cycles. Uterine malformation, submucous myoma and endometrial polyps.

• Hypersensitivity against study medication. Other contraindications according to www.fass.se

• Development of serious disease contraindicating ART or pregnancy.

• Participation or recent participation in a clinical study with an investigational product (past 30 days). Previous participation in this study.

Related Conditions & MeSH terms

• Embryo Transfer
• Infertility

Intervention

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

Locations

Country	Name	City	State
Sweden	Department of Reproductive Medicine	Gothenburg

Sponsors (2)

Lead Sponsor	Collaborator
Vastra Gotaland Region	Göteborg University

Country where clinical trial is conducted

Sweden, 

References & Publications (1)

Duffy JMN, AlAhwany H, Bhattacharya S, Collura B, Curtis C, Evers JLH, Farquharson RG, Franik S, Giudice LC, Khalaf Y, Knijnenburg JML, Leeners B, Legro RS, Lensen S, Vazquez-Niebla JC, Mavrelos D, Mol BWJ, Niederberger C, Ng EHY, Otter AS, Puscasiu L, Ra — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with live birth	A child born alive. Also, the outcome will be reported according to Core Outcome Measure for Infertility Trials (Duffy et al., 2020) in a separate appendix.	Up to 41 weeks after embryo transfer.
Secondary	Number of participants with biochemical pregnancy	A pregnancy diagnosed only by the detection of beta hCG in serum or urine.	2-3 weeks after embryo transfer.
Secondary	Number of participants with clinical pregnancy	A pregnancy diagnosed by ultrasonographic visualization of one or more gestational sacs.	4-8 weeks after embryo transfer.
Secondary	Number of participants with ongoing pregnancy	An intrauterine pregnancy with one or more fetuses with heartbeats measured in gestational week 7+5 to 9+0 with vaginal ultrasound.	5-7 weeks after embryo transfer.
Secondary	Number of participants with miscarriage	The spontaneous loss of an intra-uterine pregnancy prior to 22 completed weeks of gestational age. Also, the outcome will be reported according to Core Outcome Measure for Infertility Trials (Duffy et al., 2020) in a separate appendix.	Up to 20 weeks after embryo transfer.
Secondary	Number of participants with ectopic pregnancy	A pregnancy outside the uterine cavity, diagnosed by ultrasound, surgical visualization, or histopathology.	Up to 20 weeks after embryo transfer.
Secondary	Number of participants with termination of pregnancy	Defined as the termination of a clinical pregnancy, by deliberate interference that takes place before 22 completed weeks of gestational age. Also, the outcome will be reported according to Core Outcome Measure for Infertility Trials (Duffy et al., 2020) in a separate appendix.	Up to 20 weeks after embryo transfer.
Secondary	Birth weight	Defined as weight in grams at birth.	Up to 41 weeks after embryo transfer.
Secondary	Gestational age at delivery	The gestational age at FET is calculated by adding the number of culture days to ovulation (ovulation=day 14). Gestational age at delivery is then calculated by adding the number of days since FET.	Up to 41 weeks after embryo transfer.
Secondary	Preterm birth	Defined as a child born alive before 37 completed weeks of pregnancy.	Up to 35 weeks after embryo transfer.
Secondary	Very preterm birth	Defined as a child born alive before 32 completed weeks of pregnancy.	Up to 30 weeks after embryo transfer.
Secondary	Low birth weight	Birth weight less than 2500 g.	Up to 41 weeks after embryo transfer.
Secondary	Very low birth weight	Birth weight less than 1500 g.	Up to 41 weeks after embryo transfer.
Secondary	Stillbirth	The death of a fetus prior to the complete expulsion or extraction from its mother, after and including 22 completed weeks of gestational age. Also, the outcome will be reported according to Core Outcome Measure for Infertility Trials (Duffy et al., 2020) in a separate appendix.	Up to 41 weeks after embryo transfer.
Secondary	Perinatal death	Fetal or neonatal death occurring during late pregnancy (at 22 completed weeks of gestational age and later), during childbirth, or up to seven days after birth. Also, the outcome will be reported according to Core Outcome Measure for Infertility Trials (Duffy et al., 2020) in a separate appendix.	Up to 41 weeks after embryo transfer and 7 days after birth.
Secondary	Number of children with birth defects	Congenital birth defects were defined according the International Statistical Classification of Diseases and Related Health Problems (ICD-10). And further defined according to the EUROCAT classification system.	Up to 41 weeks after embryo transfer.
Secondary	Number of children admitted to Neonatal Intensive Care Unit (NICU)	Defined as children that were admitted to NICU after birth.	Up to 41 weeks after embryo transfer and 7 days after birth.
Secondary	Number of participants with hypertensive disorders of pregnancy	Hypertensive disorders of pregnancy defined as high blood pressure disorders including preeclampsia, gestational hypertension and chronic hypertension.	Up to 41 weeks after embryo transfer including the postpartum period before discharge of mother.
Secondary	Number of participants with placenta previa	Defined as a placenta covering the internal os of the cervix, at time of delivery.	Up to 41 weeks after embryo transfer.
Secondary	Number of participants with placenta abruption	Defined as the premature separation of a normally located placenta from the uterine wall that occurs before delivery of the fetus.	Up to 41 weeks after embryo transfer.
Secondary	Number of participants with postpartum hemorrhage	Defined as a cumulative blood loss of greater than 1,000 mL or blood loss accompanied by signs or symptoms of hypovolemia within 24 hours after the birth process.	Up to 41 weeks after embryo transfer.
Secondary	Number of participants with Cesarean section	Defined as a surgical procedure used to deliver a baby through incisions in the abdomen and uterus.	Up to 41 weeks after embryo transfer.
Secondary	Number of participants with thromboembolic events	Defined as formation in a blood vessel of a clot (thrombus) that breaks loose and is carried by the blood stream to plug another vessel.	Up to 41 weeks after embryo transfer including the postpartum period before discharge of mother.
Secondary	Maternal mortality	Defined as female deaths from any cause related to or aggravated by pregnancy or its management (excluding accidental or incidental causes) during pregnancy and childbirth.	Up to 41 weeks after embryo transfer including the postpartum period before discharge of mother.
Secondary	Number of participants with treatment related side effects	Side effects reported according to study specific questionnaire. Questions are answered with yes or no. If yes, symptoms are described, but not by using a scale.	Up to 8 weeks after embryo transfer.
Secondary	Number of participants with adverse events	Any untoward medical occurrence in symptom or disease temporally associated with the use of the medicinal (investigational) product, whether or not related to the medicinal product.	Up to 8 weeks after embryo transfer.
Secondary	Cost effectiveness	Comparison between groups regarding the total costs for the intervention divided by treatment efficacy (live birth).	After study completion, an average of 1 year.

External Links

•   EUROCAT classification system