Laparoscopic Fascial Duplication Plus Sacral Colpopexy in Posterior Vaginal Prolapse
Primary Purpose
Pelvic Organ Prolapse, Posterior Vaginal Wall Prolapse
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Laparoscopic Fascial Posterior Vagina Duplication
Sponsored by
About this trial
This is an interventional treatment trial for Pelvic Organ Prolapse
Eligibility Criteria
Age ≤ 80 years Patient's informed consent American Society of Anesthesiologists: < class III or IV
No previous major abdominal surgical procedures POP-Q stage > or =III for posterior compartment. No uterine cervix dysplasia or endometrial disorders. No uterine size larger than conform 10 weeks gestation
Sites / Locations
- Pia Fondazione Panico
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Duplication plus LSC
LSC
Arm Description
Laparoscopic duplication of posterior vagina plus mesh placement
Laparoscopic Sacral Colpopexy with mesh placement on posterior vagina
Outcomes
Primary Outcome Measures
POP-Q
POP-Q evaluation
Secondary Outcome Measures
Full Information
NCT ID
NCT05252637
First Posted
February 13, 2022
Last Updated
February 13, 2022
Sponsor
Azienda Ospedaliera Cardinale G. Panico
1. Study Identification
Unique Protocol Identification Number
NCT05252637
Brief Title
Laparoscopic Fascial Duplication Plus Sacral Colpopexy in Posterior Vaginal Prolapse
Official Title
Laparoscopic Fascial Duplication Plus Sacral Colpopexy in Posterior Vaginal Prolapse: a Randomized Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
January 20, 2021 (Actual)
Study Completion Date
January 20, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliera Cardinale G. Panico
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
A Randomized Clinical Trial on Laparoscopic Fascial posterior vaginal duplication with absorbable sutures plus sacral colpopexy mesh placement VS sacral colpopexy isolated for vaginal posterior prolapse
Detailed Description
Laparoscopic sacral colpopexy is the gold standard procedure for pelvic organ prolapse. Anyway, vaginal fascial surgery is already considered the most appropriate for posterior vaginal prolapse. This prospective randomized pilot study is aimed to verify if the combination of laparoscopic duplication of vaginal fascia with absorbable sutures could increase benefits of sacral colpopexy on the posterior vagina in terms of prolapse (evaluating 1 year POP-Q).
Secondary endpoints of this comparison are incidence of intra- or postoperative complications estimated blood loss, postoperative pain (evaluated by VAS), days of hospitalization and costs for the health care system.
Statistical Analysis and Study Design This is a single Institution prospective randomized clinical trial conducted at the Pia Fondazione Panico of Tricase, Italy.
To have an imbalanced results and to reduce any bias, a randomization list has been checked.
Probability (p) values will be considered to be statistically significant at the <0.05 level.
There will be recruited 32 patients for Groups. Group 1: Laparoscopic Fascial posterior vaginal duplication with absorbable sutures plus sacral colpopexy mesh placement Vs Group 2: Laparoscopic sacral colpopexy isolated for vaginal posterior prolapse.
All patients will be adequately informed and inserted in the study only after having read and signed an informed consent. Diagnostic, clinical and surgical data of each patient will be prospectively recorded. At the end of the procedure, a schedule will be compiled with intraoperative data. All clinical and histologic data will be recorded prospectively using a database. Pain associated with the procedure will be evaluated by a subjective assessment (analysis of VAS scale values reported by patients at 8 and 24 hours after surgery). Post-operative complications will be evaluated during the first 30 days after surgery according to Dindo's classification.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pelvic Organ Prolapse, Posterior Vaginal Wall Prolapse
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
64 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Duplication plus LSC
Arm Type
Experimental
Arm Description
Laparoscopic duplication of posterior vagina plus mesh placement
Arm Title
LSC
Arm Type
No Intervention
Arm Description
Laparoscopic Sacral Colpopexy with mesh placement on posterior vagina
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic Fascial Posterior Vagina Duplication
Intervention Description
Laparoscopic Fascial Posterior Vagina Duplication with absorbable sutures for posterior prolapse (plus standard Sacral Colpopexy)
Primary Outcome Measure Information:
Title
POP-Q
Description
POP-Q evaluation
Time Frame
1 year
10. Eligibility
Sex
Female
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Age ≤ 80 years Patient's informed consent American Society of Anesthesiologists: < class III or IV
No previous major abdominal surgical procedures POP-Q stage > or =III for posterior compartment. No uterine cervix dysplasia or endometrial disorders. No uterine size larger than conform 10 weeks gestation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Morciano
Organizational Affiliation
Pia Fondazione Panico
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pia Fondazione Panico
City
Tricase
State/Province
Lecce
ZIP/Postal Code
73039
Country
Italy
12. IPD Sharing Statement
Learn more about this trial
Laparoscopic Fascial Duplication Plus Sacral Colpopexy in Posterior Vaginal Prolapse
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