NCT07170137

Brief Summary

Comparison of differences in distension by volumetric analysis of the uterus before and after distension between groups of infertile and apparently fertile women.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 15, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

September 5, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 12, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 15, 2025

Completed
Last Updated

September 12, 2025

Status Verified

September 1, 2025

Enrollment Period

4 months

First QC Date

September 5, 2025

Last Update Submit

September 5, 2025

Conditions

Infertile Women Undergoing IVF or ICSIDistension by Volumetric Analysis of the Uterus

Outcome Measures

Primary Outcomes (1)

  • uterine distension

    1 years

Study Arms (2)

infertile women

fertile women

Eligibility Criteria

Age18 Years - 43 Years
Sexfemale
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

women seeking assisted reproductive technology (ART)

You may qualify if:

  • Patient age ≥ 18 and \< 43 years old
  • No contraindications to pregnancy
  • Patients consulting at the Saint Denis assisted reproductive technology (ART) department due to desire to become pregnant or infertility

You may not qualify if:

  • Contraindication to assisted reproductive technology treatment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre hospitalier Delafontaine

Saint-Denis, 93200, France

RECRUITING

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 5, 2025

First Posted

September 12, 2025

Study Start

July 15, 2025

Primary Completion

November 15, 2025

Study Completion

November 15, 2025

Last Updated

September 12, 2025

Record last verified: 2025-09

Locations

FR(1)