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Clinical Trials/NCT06072456
NCT06072456
Completed
Not Applicable

Comparison of Vaginal Axis on MRI in Alternative Apical Prolapse Surgeries to Sacrocolpopexy

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization2 sites in 1 country60 target enrollmentAugust 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pelvic Organ Prolapse
Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Enrollment
60
Locations
2
Primary Endpoint
Vaginal axis
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Sacrocolpopexy remains the preeminent modality in addressing apical prolapse surgically. Nevertheless, amplified morbidity rates within cohorts characterized by obesity and advanced age constrain the advantages conferred by the procedure. Recent years have witnessed a proliferation of inquiries appraising the efficacy of laparoscopic lateral suspension, pectopexy, and sacrospinous ligament fixation interventions, which have, over time, garnered extensive clinical application, in relation to recurrence rates. A multitude of investigations have been undertaken to delineate the optimal vaginal axis. In the present investigation, we have delineated a research protocol aimed at scrutinizing these alternative surgical modalities with regard to their impact on the vaginal axis.

Detailed Description

The study objective pertains to the assessment of vaginal axis in patients undergoing apical prolapse surgery, whether they have undergone hysterectomy or not. The investigation is designed to test the null hypothesis by means of a comparative analysis of preoperative and postoperative Magnetic Resonance Imaging images capturing the vaginal axis. This examination will be conducted on patients slated to receive lateral mesh suspension, pectopexy, and sacrospinous ligament fixation procedures for the correction of apical prolapse.

Registry
clinicaltrials.gov
Start Date
August 1, 2023
End Date
December 27, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Responsible Party
Principal Investigator
Principal Investigator

fatih sahin

Principal Investigator, MD

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Eligibility Criteria

Inclusion Criteria

  • Female with 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

Outcomes

Primary Outcomes

Vaginal axis

Time Frame: at 4th months after the operation

From the images obtained in the sagittal plane, the vagina, which will be observed as a high signal intensity linear structure in T2A images, and the levator plate extending as a flow-signal intensity flat structure in T1A images, will be evaluated.

Vaginal distances

Time Frame: at 4th months after the operation

The distance between the posterior vaginal fornix and the midpoint of the anterior side of the 2nd vertebra will be measured in the mid-sagittal plane (PF-S2). The distance between the right spina ischiadica and right vaginal fornix (RSI-RF), and, the distance between the left spina ischiadica and left vaginal fornix (LSI-LF) will be measured on T2A images acquired in the axial plane.

Secondary Outcomes

  • Prolapse symptoms, Colorectal-Anal Impact Questionnaire(at 4th months after the operation)
  • Prolapse symptoms(at 4th months after the operation)
  • Quality of life measures(at 4th months after the operation)
  • Urinary Symptoms(at 4th months after the operation)
  • Postoperative de novo dyspareunia(at 4th months after the operation)
  • Sexual functions(at 4th months after the operation)
  • Patient Global Impression of Improvement (PGI-I)(at 4th months after the operation)

Study Sites (2)

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