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Clinical and Urodynamic Evaluation of Surgical Repair of Pelvic Organ Prolapse Associated With Lower Urinary Tract Symptoms

Primary Purpose

Pelvic Organ Prolapse

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Urodynamic study
Sponsored by
Ain Shams University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Pelvic Organ Prolapse

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • women with anterior pelvic organ prolapse (POP) associated with Lower urinary tract symptoms

Exclusion Criteria:

  • Patients with POP less than POP-Q grade II, POP not in need for surgical repair, neurological diseases that could possibly affect voiding functions, pelvic infections, congenital bladder disorders, history of urinary fistula, history of malignancy, and patients on current medical treatment for voiding dysfunction.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Urodynamic study evaluation for the participants
    evaluation of the urodynamic study after the surgical repair of the pelvic organ prolapse and comparison to the preoperative results.

    Secondary Outcome Measures

    Full Information

    First Posted
    March 9, 2021
    Last Updated
    March 9, 2021
    Sponsor
    Ain Shams University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04793126
    Brief Title
    Clinical and Urodynamic Evaluation of Surgical Repair of Pelvic Organ Prolapse Associated With Lower Urinary Tract Symptoms
    Official Title
    Clinical and Urodynamic Evaluation of Surgical Repair of Pelvic Organ Prolapse Associated With Lower Urinary Tract Symptoms
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2021
    Overall Recruitment Status
    Completed
    Study Start Date
    December 1, 2014 (Actual)
    Primary Completion Date
    July 1, 2016 (Actual)
    Study Completion Date
    December 1, 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Ain Shams University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    To assess the urinary symptoms and urodynamic findings concomitant with Pelvic organ prolapse before and after surgical treatment and to define the role of urodynamic study in treatment decision making.
    Detailed Description
    Pelvic organ prolapse (POP) is a prevalent problem that affects women's quality of life women with POP may present with a variety of lower urinary tract symptoms (LUTS). For POP patients with concomitant urinary symptoms, urodynamic (UDN) testing is proposed for proper evaluation of cases and identification of the pathophysiologic events in each case individually. In this prospective study, the investigators aim to describe the urinary symptoms and urodynamic findings concomitant with POP before and after surgical treatment of POP. We also aimed at defining the role of UDN in decision-making regarding the treatment of POP when associated with LUTS.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pelvic Organ Prolapse

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Phase 2
    Interventional Study Model
    Single Group Assignment
    Model Description
    All patients were subjected to clinical evaluation and urodynamic testing before surgery. All cases underwent surgical repair of pelvic organ prolapse. Follow-up clinical examination was performed at 1, 3, and 6 months postoperatively, and urodynamic examination was repeated 6 months after repair.
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    83 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Urodynamic study
    Intervention Description
    comparison between the urodynamic study of the patients before pelvic prolapse surgical repair and 6 months later.
    Primary Outcome Measure Information:
    Title
    Urodynamic study evaluation for the participants
    Description
    evaluation of the urodynamic study after the surgical repair of the pelvic organ prolapse and comparison to the preoperative results.
    Time Frame
    6 month after the procedure

    10. Eligibility

    Sex
    Female
    Gender Based
    Yes
    Gender Eligibility Description
    Pelvic organ prolapse surgeries
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: women with anterior pelvic organ prolapse (POP) associated with Lower urinary tract symptoms Exclusion Criteria: Patients with POP less than POP-Q grade II, POP not in need for surgical repair, neurological diseases that could possibly affect voiding functions, pelvic infections, congenital bladder disorders, history of urinary fistula, history of malignancy, and patients on current medical treatment for voiding dysfunction.

    12. IPD Sharing Statement

    Learn more about this trial

    Clinical and Urodynamic Evaluation of Surgical Repair of Pelvic Organ Prolapse Associated With Lower Urinary Tract Symptoms

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