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The Change in Vaginal Axis on MRI After Uterus Preserving Laparoscopic Lateral Mesh Suspension

S

Sisli Hamidiye Etfal Training and Research Hospital

Status

Completed

Conditions

Prolapse Genital
Anatomical Pathological Condition

Treatments

Diagnostic Test: Magnetic resonance imaging

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Laparoscopic lateral mesh suspension is emerged as a practical, safe and feasible alternative to sacropexy to treat female genital apical prolapse. Investigators hypothesized that uterus-preserving lateral suspension provides a better anatomical positioning.

Full description

Suspending the cervix to the bilateral abdominal wall through subperitoneal tunnels may properly mimic cardinal ligament and restore the normal vaginal axis. To prove the null hypothesis, it is planned to compare the vaginal axis on Magnetic Resonans Imaging taken preoperatively and postoperatively in patients who are scheduled for lateral mesh suspension for apical prolapse.

Enrollment

21 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Female genital prolapse

Exclusion criteria

  • Patients who had pouch of Douglas obliteration
  • Patients with enterocele
  • Patients who have any congenital or acquired anatomic and reproductive anomaly

Trial design

21 participants in 2 patient groups

Study
Description:
Patients who had the operation of "laparoscopic lateral mesh suspension" for apical prolapse will have magnetic resonance imaging preoperatively and at postoperative 6th month
Treatment:
Diagnostic Test: Magnetic resonance imaging
Control
Description:
Multiparous, sexually active participants who have grade 0 or 1 (asymptomatic if exists) prolapse will have magnetic resonance imaging as a control group
Treatment:
Diagnostic Test: Magnetic resonance imaging

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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