Analysis of Procedural Times Using Colpassist for Robotic-Assisted Sacrocolpopexy; a Randomized Controlled Trial (ACRAS)
Primary Purpose
Pelvic Organ Prolapse
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Traditional vaginal positioning device
Colpassist vaginal positioning device
Sponsored by
About this trial
This is an interventional treatment trial for Pelvic Organ Prolapse focused on measuring robotic, sacrocolpopexy, Colpassist, vaginal positioning device
Eligibility Criteria
Inclusion Criteria:
- Age greater than or equal to 18 years old
- Planned robotic-assisted sacrocolpopexy
- English speaking
- Prior hysterectomy (either total or supra-cervical)
Exclusion Criteria:
- Age less than 18 years old
- Non-English speaking
- Pregnant women, or women desiring future pregnancy
- Planned concomitant hysterectomy
Sites / Locations
- University of North Carolina, Chapel Hill - Female Pelvic Medicine and Reconstructive Surgery
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Traditional vaginal positioning device
Colpassist vaginal positioning device
Arm Description
Patients will undergo their robotic-assisted sacrocolpopexy using a vaginally placed endo anal sizer.
Patients will undergo their robotic-assisted sacrocolpopexy using a vaginally placed Colpassist vaginal manipulator.
Outcomes
Primary Outcome Measures
Comparison of duration of surgical steps during sacral colpopexy
Length of time will be recorded for each step of the sacral colpopexy that utilizes the vaginal positioning device (dissection of anterior vaginal wall, dissection of posterior vaginal wall, attachment of anterior vaginal mesh, attachment of posterior vaginal mesh, and attachment of sacral mesh) during the surgery. No follow up will be required by the patient.
Secondary Outcome Measures
Surgeon and surgical-assistant satisfaction with the device
Surgeon and surgical assistant satisfaction will be assessed via questionnaire immediately after surgery. No follow up will be required of the surgeons or the assistants.
Full Information
NCT ID
NCT02367235
First Posted
December 9, 2014
Last Updated
April 25, 2018
Sponsor
University of North Carolina, Chapel Hill
Collaborators
Boston Scientific Corporation, Intuitive Surgical
1. Study Identification
Unique Protocol Identification Number
NCT02367235
Brief Title
Analysis of Procedural Times Using Colpassist for Robotic-Assisted Sacrocolpopexy; a Randomized Controlled Trial
Acronym
ACRAS
Official Title
Analysis of Robotic Procedural Times Using the Colpassist Vaginal Positioning Device for Robotic-Assisted Sacrocolpopexy; a Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
April 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
Boston Scientific Corporation, Intuitive Surgical
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the efficiency of the Colpassist vaginal positioning device during robotic-assisted sacrocolpopexy.
Detailed Description
The purpose of this research study is to evaluate the efficiency of the Colpassist (Boston Scientific, Natick, MA) vaginal positioning device used during robotic-assisted sacrocolpopexy. Traditionally, vaginal positioning during robotic-assisted sacrocolpopexy is done using a device that was not designed specifically for sacrocolpopexy, commonly a vaginally placed endo anal sizer. It is possible the Colpassist device will result in shorter operative times because Colpassist is flat which makes it easier to sew against. Also, the width of the device is designed to be similar to the width of the vagina which should improve visibility during surgery.
Enrolled patients will be randomized to undergo their planned robotic-assisted sacrocolpopexy using either a vaginally placed endo anal sizer or a vaginally placed Colpassist vaginal positioning device. Both surgeon and patient will be blinded to which device was used at the time of surgery. Length of time to complete each step of the sacral colpoexy that involves use of a vaginal positioning device (dissection of the anterior and posterior vaginal walls, attachment of anterior and posterior vaginal mesh, attachment of sacral mesh) will be recorded during the surgery to measure operative efficiency. Surgeon and surgical-assistant satisfaction will be recorded with each device.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pelvic Organ Prolapse
Keywords
robotic, sacrocolpopexy, Colpassist, vaginal positioning device
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
52 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Traditional vaginal positioning device
Arm Type
Experimental
Arm Description
Patients will undergo their robotic-assisted sacrocolpopexy using a vaginally placed endo anal sizer.
Arm Title
Colpassist vaginal positioning device
Arm Type
Experimental
Arm Description
Patients will undergo their robotic-assisted sacrocolpopexy using a vaginally placed Colpassist vaginal manipulator.
Intervention Type
Procedure
Intervention Name(s)
Traditional vaginal positioning device
Intervention Description
A vaginally placed endo-anal sizer will be used to position the vagina during surgery.
Intervention Type
Procedure
Intervention Name(s)
Colpassist vaginal positioning device
Intervention Description
A vaginally placed Colpassist will be used to position the vagina during surgery.
Primary Outcome Measure Information:
Title
Comparison of duration of surgical steps during sacral colpopexy
Description
Length of time will be recorded for each step of the sacral colpopexy that utilizes the vaginal positioning device (dissection of anterior vaginal wall, dissection of posterior vaginal wall, attachment of anterior vaginal mesh, attachment of posterior vaginal mesh, and attachment of sacral mesh) during the surgery. No follow up will be required by the patient.
Time Frame
Intraoperative
Secondary Outcome Measure Information:
Title
Surgeon and surgical-assistant satisfaction with the device
Description
Surgeon and surgical assistant satisfaction will be assessed via questionnaire immediately after surgery. No follow up will be required of the surgeons or the assistants.
Time Frame
On the day of surgery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age greater than or equal to 18 years old
Planned robotic-assisted sacrocolpopexy
English speaking
Prior hysterectomy (either total or supra-cervical)
Exclusion Criteria:
Age less than 18 years old
Non-English speaking
Pregnant women, or women desiring future pregnancy
Planned concomitant hysterectomy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth Geller, MD
Organizational Affiliation
UNC-Chapel Hill
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of North Carolina, Chapel Hill - Female Pelvic Medicine and Reconstructive Surgery
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Analysis of Procedural Times Using Colpassist for Robotic-Assisted Sacrocolpopexy; a Randomized Controlled Trial
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