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NCT07450300Completed

Assessment of the Feasibility of Frozen Embryo Transfers in a Natural Cycle Among Obese Compared to Non-Obese Patients

Source: ClinicalTrials.gov · Last updated 4 Mar 2026

Brief summary (registry, in English)

This retrospective study included 1,831 single blastocyst frozen embryo transfer (FET) cycles performed between November 1, 2022 and August 31, 2025. Three endometrial preparation protocols were used according to ovulatory status, cycle duration, and characteristics of previous FET cycles: modified natural cycle with ovulation trigger (mNC-FET) (n = 770), stimulated cycle FET (SC-FET) (n = 468), and hormone replacement therapy FET (HRT-FET) (n = 593). In natural cycles, if the predefined criteria for ovulation trigger were not met, the cycle was converted to a stimulated cycle. The aim of this study was to determine whether body mass index affects embryo transfer feasibility, reproductive outcomes, and cycle characteristics across different FET protocols.

Status (registry)
Completed
Study type
Observational
Enrollment
1831 (actual)
First submitted
19 Feb 2026
Start date
1 Nov 2022
Primary completion date
31 Aug 2025
Lead sponsor
Clinique Mathilde
Diseases
Obesity
NCT number
NCT07450300

What you commit to

  • Study type: Observational
  • Participants enrolled: 1831
  • From 1 Nov 2022 to the primary completion date, 31 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Women aged ≥18 years at the time of frozen embryo transfer.
  • Patients undergoing assisted reproductive technology (ART) with frozen embryo transfer (FET) using a natural, modified natural, stimulated, or hormone replacement therapy (HRT) protocol.
  • Availability of body mass index (BMI) measurement prior to initiation of the treatment cycle.

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Clinique Mathilde
Coordinator of this site? Confirm its status
RouenFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.