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Treatment of Urinary Stress Incontinence During or Following Correction of Pelvic Organ Prolapse

Primary Purpose

Pelvic Organ Prolapse

Status
Withdrawn
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
correction of POP plus preventive continence procedure
POP surgery followed by eventual incontinence procedure
Sponsored by
University Magna Graecia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pelvic Organ Prolapse focused on measuring Pelvic organ prolapse, Urinary incontinence, Mesh

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pelvic organ prolapse stage 2-3
  • Absence of subjective urinary stress incontinence

Exclusion Criteria:

  • pregnancy
  • <12 months postpartum
  • systemic disease known to affect bladder function
  • current chemotherapy or radiation therapy
  • urethral diverticulum, augmentation cytoplasty, or artificial sphincter
  • recent pelvic surgery
  • patient age under 18 and over 80
  • any previous pelvic surgery, diabetes mellitus and collagen disease

Sites / Locations

  • "Pugliese" Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

unique surgery

Double surgery

Outcomes

Primary Outcome Measures

efficacy (cure rate)

Secondary Outcome Measures

intra-operative complication rate
postoperative complications rate
sexual function
quality of life
Failure rate
Recurrence rate

Full Information

First Posted
June 12, 2008
Last Updated
April 5, 2013
Sponsor
University Magna Graecia
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1. Study Identification

Unique Protocol Identification Number
NCT00697489
Brief Title
Treatment of Urinary Stress Incontinence During or Following Correction of Pelvic Organ Prolapse
Official Title
Pelvic Organ Prolapse Correction Plus Preventive Treatment of Urinary Stress Incontinence vs. Correction of Pelvic Organ Prolapse Followed by Treatment of Urinary Stress Incontinence
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Withdrawn
Study Start Date
June 2008 (undefined)
Primary Completion Date
August 2010 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Magna Graecia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The incidence of pelvic organ prolapse (POP) in parous women is estimated over 50%. A variety of urinary, bowel and sexual symptoms may be associated with POP. Moreover, a proportion of women who underwent a surgical correction of POP may occur post-surgical urinary incontinence and, thus, if this last presents as genuine stress-type or mixed-type, a second surgical intervention may be required. At this proposal, with the aim to reduce the incidence of postoperative urinary incontinence, the addition of a preventive continence procedure to a POP repair intervention has been widely proposed, but the potential benefits needs to be balanced against potential disadvantages. Based on these considerations, the aim of this trial will be to compare two different surgical strategies for women with POP without urinary stress incontinence. Specifically, the efficacy to associate and to follow a preventive continence procedure to the correction of POP will be compared.
Detailed Description
Women with POP not associated to urinary stress incontinence will be enrolled and randomized in two arms(groups A and B). Patients of group A will be treated with unique surgery (correction of POP plus preventive continence procedure), whereas in patients of group B POP will be surgically corrected and, in case of stress or mixed postoperative incontinence, a further intervention for urinary stress incontinence will be tailored. All patients eligible will undergo baseline assessment consisting of anthropometric, clinical, hormonal, ultrasonographic and urodynamic evaluations. During the study, the clinical outcomes, and the adverse experience will be evaluated in each patient. Data will be analyzed using the intention-to-treat principle and a P value of 0.05 or less will be considered significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pelvic Organ Prolapse
Keywords
Pelvic organ prolapse, Urinary incontinence, Mesh

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
unique surgery
Arm Title
2
Arm Type
Active Comparator
Arm Description
Double surgery
Intervention Type
Procedure
Intervention Name(s)
correction of POP plus preventive continence procedure
Intervention Type
Procedure
Intervention Name(s)
POP surgery followed by eventual incontinence procedure
Primary Outcome Measure Information:
Title
efficacy (cure rate)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
intra-operative complication rate
Time Frame
one day
Title
postoperative complications rate
Time Frame
12 months
Title
sexual function
Time Frame
12 months
Title
quality of life
Time Frame
12 months
Title
Failure rate
Time Frame
12 months
Title
Recurrence rate
Time Frame
12 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pelvic organ prolapse stage 2-3 Absence of subjective urinary stress incontinence Exclusion Criteria: pregnancy <12 months postpartum systemic disease known to affect bladder function current chemotherapy or radiation therapy urethral diverticulum, augmentation cytoplasty, or artificial sphincter recent pelvic surgery patient age under 18 and over 80 any previous pelvic surgery, diabetes mellitus and collagen disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefano Palomba, MD
Organizational Affiliation
Chair of Obstetrics and Gynecology, University "Magna Graecia" of Catanzaro
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Fulvio Zullo, MD
Organizational Affiliation
Chair of Obstetrics and Gynecology, University "Magna Graecia" of Catanzaro
Official's Role
Study Chair
Facility Information:
Facility Name
"Pugliese" Hospital
City
Catanzaro
ZIP/Postal Code
88100
Country
Italy

12. IPD Sharing Statement

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Treatment of Urinary Stress Incontinence During or Following Correction of Pelvic Organ Prolapse

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