Sexual Intercourse and Vaginal Absorption of Progesterone
- Conditions
- Infertility
- Interventions
- Behavioral: Sexual event
- Registration Number
- NCT05232344
- Lead Sponsor
- University Hospital, Montpellier
- Brief Summary
The objective of this project is to compare the vaginal absorption of progesterone administered in the vaginal ovum by measuring progesteroneemia in 3 situations (or "sexual event"): abstinence, sex protected by condoms and unprotected sex.
- Detailed Description
Progesterone plays a key role in embryo implantation and maintenance of pregnancy.
In the context of Assisted Reproduction (ART), support for the luteal phase is often necessary and readily provided by the administration of progesterone, mainly vaginal in Europe.
Optimal absorption is essential because low progesterone levels are associated with the chances of lowered pregnancies.
However, it has been shown that vaginal absorption can be reduced following unprotected sex.
Would the use of a condom prevent this alteration of vaginal absorption?
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- Couples, volunteers, on an AMP journey
- Having sexual intercourse with a low risk of transmission of sexually transmitted infection
- Free and informed consent to participate in the study
Inclusion criteria specific to women:
- aged 18 to 40 inclusive
Exclusion criteria specific to women:
- Currently taking hormone therapy that may alter progesteroneemia
- Pathology that can modify progesteroneemia
- Body mass index greater than or equal to 32 kg / m2
- Contraindication to the use of hormone replacement therapy
- Known intolerance to vaginal progesterone
- Pregnant woman (βHCG assay positive) or breastfeeding
Exclusion criteria specific to men:
- Erectile or ejaculatory disorder
Exclusion criteria specific to couples:
- Person with poor oral and/or written French comprehension
- Person who for psychological, social, family or geographical reasons could not be followed regularly
- Vulnerable person (Article L1121-6 of the Public Health Code)
- Protected person or unable to give consent
- Person involvment in another clinical research
- Person not affiliated with a French social security scheme or beneficiary of such a scheme
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Estradiol / Progesterone treatment Sexual event Estradiol (Provames®, 3 mg morning and evening, or 6 mg per day) Vaginal progesterone (400 mg, Progestan®, evening and morning, ie 800 mg per day). Estradiol / Progesterone treatment Estradiol / Progesterone Estradiol (Provames®, 3 mg morning and evening, or 6 mg per day) Vaginal progesterone (400 mg, Progestan®, evening and morning, ie 800 mg per day).
- Primary Outcome Measures
Name Time Method Progesterone dosage 1 Change from Baseline progesterone (Day 2) at Day 3 Change from baseline plasma progesterone (day 2), 11 hours after administration of progesterone vaginal capsules (400 mg) and protected or unprotected intercourse within one hour of progesterone administration, at day 3
Progesterone dosage 2 Change from Baseline progesterone (Day 2) at Day 7 Change from baseline plasma progesterone (day 2), 11 hours after administration of progesterone vaginal capsules (400 mg) and protected or unprotected intercourse within one hour of progesterone administration, at day 7
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
CHU de Montpellier
🇫🇷Montpellier, France