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Prospective Study of the Variation in the Angle of Anteflexion of the Uterus Before and After Micturition in Nulliparous Women With Uterine Anteversion. (FLEXIMIX)

R

Regional University Hospital Center (CHRU)

Status

Completed

Conditions

Uterine Anteflexion

Treatments

Procedure: Ultrasonography, Pelvic

Study type

Interventional

Funder types

Other

Identifiers

NCT06669845
29BRC24.0124
2024-A01255-42 (Other Identifier)

Details and patient eligibility

About

A monocentric, prospective, comparative, and descriptive clinical study examining the uterine anteflexion angle before and after bladder emptying in nulliparous women with uterine anteversion. The study aims to assess how bladder fullness affects the anteflexion angle, which may impact the ease of intrauterine device (IUD) insertion. The primary objective is to determine the variation in the angle of anteflexion of the uterus before and after micturition in nulliparous women with uterine anteversion. Ultrasound measurements will be taken before and after bladder emptying. A secondary objective is to determine the prevalence of uterine anteversion in nulliparous women.

Enrollment

250 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women aged 18 and over;
  • Nulliparous ;
  • Feeling the need to urinate;
  • Affiliated to a Social Security scheme.

Exclusion criteria

  • Pregnant women;
  • Desire of pregnancy with conception in progress;
  • Primary amenorrhea ;
  • Menopause ;
  • Previous surgical termination of pregnancy;
  • Previous medical abortion;
  • Previous hysterectomy ;
  • Previous conization;
  • Absence of uterus;
  • Irrepressible need to urinate;
  • Inability or refusal to participate in the study.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

250 participants in 1 patient group

Ultrasonography pelvic
Other group
Description:
Ultrasound measurements before and after bladder emptying
Treatment:
Procedure: Ultrasonography, Pelvic

Trial contacts and locations

1

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Central trial contact

Audrey LE GOFF COQUET; CHIRON BENOIT, MD

Data sourced from clinicaltrials.gov

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