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Trial Comparing Laparoscopic Vs Robotic-assisted Colposacropexy for Pelvic Organ Prolapse Repair

Primary Purpose

Pelvic Organ Prolapse

Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
sacrocolpopexy
Sponsored by
University Of Perugia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pelvic Organ Prolapse focused on measuring Laparoscopic Sacrocolpopexy, Robotic Assisted Sacrocolpopexy, Pelvic Organ Prolapse

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Symptomatic POP >2 stage according to POP Q system

Exclusion Criteria:

  • Obesity
  • Heart failure (NYHA III-IV)
  • High stage COPD (Chronic Obstructive Pulmonary Disease)
  • Patients who underwent more than 2 previous abdominal surgical procedures

Sites / Locations

  • Santa Maria della Misericordia Hospital- University of PerugiaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Laparoscopic sacrocolpopexy

Robotic assisted Sacrocolpopexy

Arm Description

The surgical technique will be the same between the two approaches, in this arm the approach will be laparoscopic

The surgical technique will be the same between the two approaches, in this arm the approach will be robotic assisted

Outcomes

Primary Outcome Measures

Anatomical outcome
POP <2 according to POP-Q system

Secondary Outcome Measures

Intraoperative ando post operative complications
Clavien-Dindo classification of surgery complications
post operative pain
VAS score (Visual Analog Pain Scale)
voiding and storage symptoms
fill in Urinary Distress Inventory short form (UDI-6) to assess urinary symptoms
sexual dysfunctions
fill in Female Sexual Function Index questionnaire (FSFI)
patient satisfaction
fill in Patient Global Impression of Improvement (PGI-I)
Quality of life
fill in Incontinence Impact Questionnaire-Short form (IIQ-7)

Full Information

First Posted
July 26, 2016
Last Updated
August 3, 2016
Sponsor
University Of Perugia
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1. Study Identification

Unique Protocol Identification Number
NCT02852512
Brief Title
Trial Comparing Laparoscopic Vs Robotic-assisted Colposacropexy for Pelvic Organ Prolapse Repair
Official Title
Perspective Randomized Trial Comparing Laparoscopic Vs Robotic-assisted Colposacropexy for Pelvic Organ Prolapse Repair
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2016 (undefined)
Primary Completion Date
March 2017 (Anticipated)
Study Completion Date
March 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Of Perugia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is to perspectively compare the anatomical and functional outcomes of Pelvic Organ Prolapse (POP) repair after Laparoscopic or Robotic-assisted Colposacropexy.
Detailed Description
Female pelvic floor disorders rank amongst the most common disorders affecting women and include conditions such as urinary incontinence and pelvic organ prolapse (POP). POP is estimated to affect 30% of women aged 50- 89 years, and the lifetime risk of requiring surgery is 11%. Open abdominal sacrocolpopexy is the established gold standard procedure and is indicated when there is prolapse of the anterior and/or apical vaginal wall compartments. Laparoscopic sacrocolpopexy (LSCP) has not been widely adopted as it demands skill and motivation and it is associated with a long learning curve. So the hypothesis is that robot-assisted laparoscopic approach for sacrocolpopexy (RALSCP) could be an alternative to a pure laparoscopic technique. In the study design 62 patients will be randomly enrolled (31 in the laparoscopic arm and 31 in the robotic assisted one). The primary outcome will be the anatomic one, secondary outcomes will be functional in terms of storage or voiding dysfunctions, sexual dysfunctions, bowel dysfunctions, QoL, post operative complications. For continuous variables will be used the Mann-Withney test, for categorical data will be used McNemar test and X2 test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pelvic Organ Prolapse
Keywords
Laparoscopic Sacrocolpopexy, Robotic Assisted Sacrocolpopexy, Pelvic Organ Prolapse

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
62 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Laparoscopic sacrocolpopexy
Arm Type
Active Comparator
Arm Description
The surgical technique will be the same between the two approaches, in this arm the approach will be laparoscopic
Arm Title
Robotic assisted Sacrocolpopexy
Arm Type
Active Comparator
Arm Description
The surgical technique will be the same between the two approaches, in this arm the approach will be robotic assisted
Intervention Type
Procedure
Intervention Name(s)
sacrocolpopexy
Intervention Description
Peritoneal incision from the sacral promontory to the Pouch of Douglas. After careful dissection of the inter-rectovaginal space, a two-piece Y-shaped polypropylene mesh was fixed posteriorly to the levator ani muscles using a absorbable suture. The midpoint of the mesh is anchored to the posterior wall of the vagina. The anterior portion of mesh was then introduced and fixed within the intervesico- vaginal space to the anterior/apical vaginal wall with a running suture. The tails of both meshes were fixed to the sacral promontory with a strong non-absorbable polypropylene suture. The peritoneal incision was re- approximated with a running absorbable suture
Primary Outcome Measure Information:
Title
Anatomical outcome
Description
POP <2 according to POP-Q system
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Intraoperative ando post operative complications
Description
Clavien-Dindo classification of surgery complications
Time Frame
during surgery and within 90 days after surgery
Title
post operative pain
Description
VAS score (Visual Analog Pain Scale)
Time Frame
within 7 days after surgery
Title
voiding and storage symptoms
Description
fill in Urinary Distress Inventory short form (UDI-6) to assess urinary symptoms
Time Frame
2, 6, 12 months after surgery
Title
sexual dysfunctions
Description
fill in Female Sexual Function Index questionnaire (FSFI)
Time Frame
2, 6, 12 months after surgery
Title
patient satisfaction
Description
fill in Patient Global Impression of Improvement (PGI-I)
Time Frame
12 months after surgery
Title
Quality of life
Description
fill in Incontinence Impact Questionnaire-Short form (IIQ-7)
Time Frame
2, 6, 12 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Symptomatic POP >2 stage according to POP Q system Exclusion Criteria: Obesity Heart failure (NYHA III-IV) High stage COPD (Chronic Obstructive Pulmonary Disease) Patients who underwent more than 2 previous abdominal surgical procedures
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elisabetta Costantini, MD
Phone
+393393384370
Email
elisabetta.costantini@unipg.it
First Name & Middle Initial & Last Name or Official Title & Degree
Ester Illiano, MD
Phone
+393283620614
Email
ester.illiano@inwind.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elisabetta Costantini, MD
Organizational Affiliation
University Of Perugia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Santa Maria della Misericordia Hospital- University of Perugia
City
Perugia
ZIP/Postal Code
06100
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elisabetta Costantini, MD
Phone
+393393384370
Email
elisabetta.costatini@unipg.it
First Name & Middle Initial & Last Name & Degree
Ester Illiano, MD
Phone
+393283620614
Email
ester.illiano@inwind.it

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24433811
Citation
Lee RK, Mottrie A, Payne CK, Waltregny D. A review of the current status of laparoscopic and robot-assisted sacrocolpopexy for pelvic organ prolapse. Eur Urol. 2014 Jun;65(6):1128-37. doi: 10.1016/j.eururo.2013.12.064. Epub 2014 Jan 8.
Results Reference
result
PubMed Identifier
21858540
Citation
Seror J, Yates DR, Seringe E, Vaessen C, Bitker MO, Chartier-Kastler E, Roupret M. Prospective comparison of short-term functional outcomes obtained after pure laparoscopic and robot-assisted laparoscopic sacrocolpopexy. World J Urol. 2012 Jun;30(3):393-8. doi: 10.1007/s00345-011-0748-2. Epub 2011 Aug 20.
Results Reference
result
PubMed Identifier
23274792
Citation
Awad N, Mustafa S, Amit A, Deutsch M, Eldor-Itskovitz J, Lowenstein L. Implementation of a new procedure: laparoscopic versus robotic sacrocolpopexy. Arch Gynecol Obstet. 2013 Jun;287(6):1181-6. doi: 10.1007/s00404-012-2691-x. Epub 2012 Dec 30.
Results Reference
result

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Trial Comparing Laparoscopic Vs Robotic-assisted Colposacropexy for Pelvic Organ Prolapse Repair

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