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Colpopexy and Urinary Reduction Efforts (CARE) Protocol (CARE)

Primary Purpose

Urinary Incontinence, Stress, Uterine Prolapse, Vaginal Prolapse

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Burch urethropexy at time of sacrocolpopexy
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Urinary Incontinence, Stress focused on measuring Urinary incontinence, Pelvic organ prolapse, Stress incontinence, Sacrocolpopexy, Burch urethropexy, Surgical Trials

Eligibility Criteria

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

Inclusion Criteria Eligibility for primary procedure (sacrocolpopexy) Eligibility for secondary procedure (Burch colposuspension) Stage II-IV anterior vaginal prolapse, defined as POP-Q Point Aa at -1, 0, +1, +2, or +3 cm. Negative stress incontinence screen Negative stress incontinence screen (MESA questionnaire) Exclusion Criteria Contraindication for sacrocolpopexy or Burch colposuspension. Anatomic contraindication for Burch colposuspension (i.e., Point Aa fixed at -2 or -3 cm). Surgeon judgment that a contraindication to Burch colposuspension exists. Anticipated geographic relocation within the first three months after surgery (e.g., within approximately 6 months of screening). Inability to provide informed consent or to complete testing or data collection. Currently pregnant.

Sites / Locations

  • The University of Alabama at Birmingham
  • Loyola University Medical Center
  • University of Iowa College of Medicine
  • Johns Hopkins School of Medicine
  • University of North Carolina at Chapel Hill
  • Magee-Womens Hospital
  • Baylor College of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Abdominal Sacral Colpopexy with no Burch colposuspension

Abdominal Sacral Colpopexy with Burch Colposuspension

Arm Description

Abdominal sacral colpopexy is performed through a laparotomy approach.

The Burch colposuspension procedure entails the retropubic placement of at least two stitches in the vaginal tissue lateral to each side of the urethra, and suspension of these stitches from Cooper's ligament (the iliopectineal line at the superior aspect of the posterior pubic bone).

Outcomes

Primary Outcome Measures

Stress urinary continence
Patients will be categorized as stress continent or stress incontinent on the basis of symptom assessment and stress testing. The symptoms will be assessed by the stress incontinence subscale of the Pelvic Floor Distress Inventory (PFDI).

Secondary Outcome Measures

Complications at surgery
Complications at surgery
Occurrence of other lower urinary tract symptoms
measured by the urgency and obstructed voiding subscales of the PFDI
Other pelvic symptoms and health-related quality of life
includes bowel function and sexual function

Full Information

First Posted
August 1, 2003
Last Updated
January 9, 2011
Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00065845
Brief Title
Colpopexy and Urinary Reduction Efforts (CARE) Protocol
Acronym
CARE
Official Title
CARE: A Randomized Trial of Colpopexy and Urinary Reduction Efforts
Study Type
Interventional

2. Study Status

Record Verification Date
October 2010
Overall Recruitment Status
Completed
Study Start Date
April 2002 (undefined)
Primary Completion Date
March 2007 (Actual)
Study Completion Date
April 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Pelvic organ prolapse occurs when the muscles holding pelvic organs (e.g., the uterus or bladder) weaken and the organs fall or slide down into the vagina. Pelvic organ prolapse can be corrected with surgery. However, women who have this surgery may develop urinary incontinence. This study will determine how doctors can predict this problem and whether an additional surgical procedure at the time of prolapse surgery can prevent the development of urinary incontinence.
Detailed Description
Many women have surgery for pelvic organ prolapse (cystocele, uterine prolapse, rectocele). Women with advanced pelvic organ prolapse may experience stress urinary incontinence following surgery to repair the prolapse. Development of incontinence is unpredictable. This study will determine which, if any, clinical tests are useful for predicting post-operative urinary incontinence. The study will also determine if a Burch urethropexy should be performed routinely or selectively at the time of sacrocolpopexy in continent women. Women with pelvic organ prolapse who are scheduled for prolapse repair will be randomized to a Burch urethropexy group or to a control group. Women in the Burch group will undergo urethropexy at the time of prolapse repair. Assessments will include a quality of life telephone interview, urodynamic testing, and physical examination. Follow-up evaluations occur at 6 weeks, 3 months, and 1 and 2 years following surgery. Post-operative phone interviews will occur at 3 months, 6 months, and 1 and 2 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence, Stress, Uterine Prolapse, Vaginal Prolapse
Keywords
Urinary incontinence, Pelvic organ prolapse, Stress incontinence, Sacrocolpopexy, Burch urethropexy, Surgical Trials

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
322 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Abdominal Sacral Colpopexy with no Burch colposuspension
Arm Type
No Intervention
Arm Description
Abdominal sacral colpopexy is performed through a laparotomy approach.
Arm Title
Abdominal Sacral Colpopexy with Burch Colposuspension
Arm Type
Experimental
Arm Description
The Burch colposuspension procedure entails the retropubic placement of at least two stitches in the vaginal tissue lateral to each side of the urethra, and suspension of these stitches from Cooper's ligament (the iliopectineal line at the superior aspect of the posterior pubic bone).
Intervention Type
Procedure
Intervention Name(s)
Burch urethropexy at time of sacrocolpopexy
Intervention Description
The Burch colposuspension procedure entails the retropubic placement of at least two stitches in the vaginal tissue lateral to each side of the urethra, and suspension of these stitches from Cooper's ligament (the iliopectineal line at the superior aspect of the posterior pubic bone).
Primary Outcome Measure Information:
Title
Stress urinary continence
Description
Patients will be categorized as stress continent or stress incontinent on the basis of symptom assessment and stress testing. The symptoms will be assessed by the stress incontinence subscale of the Pelvic Floor Distress Inventory (PFDI).
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Complications at surgery
Description
Complications at surgery
Time Frame
2 years
Title
Occurrence of other lower urinary tract symptoms
Description
measured by the urgency and obstructed voiding subscales of the PFDI
Time Frame
3 mo, 2 years
Title
Other pelvic symptoms and health-related quality of life
Description
includes bowel function and sexual function
Time Frame
3 mo, 2 years

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Eligibility for primary procedure (sacrocolpopexy) Eligibility for secondary procedure (Burch colposuspension) Stage II-IV anterior vaginal prolapse, defined as POP-Q Point Aa at -1, 0, +1, +2, or +3 cm. Negative stress incontinence screen Negative stress incontinence screen (MESA questionnaire) Exclusion Criteria Contraindication for sacrocolpopexy or Burch colposuspension. Anatomic contraindication for Burch colposuspension (i.e., Point Aa fixed at -2 or -3 cm). Surgeon judgment that a contraindication to Burch colposuspension exists. Anticipated geographic relocation within the first three months after surgery (e.g., within approximately 6 months of screening). Inability to provide informed consent or to complete testing or data collection. Currently pregnant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Linda Brubaker, MD
Organizational Affiliation
Loyola University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233-7333
Country
United States
Facility Name
Loyola University Medical Center
City
Maywood
State/Province
Illinois
ZIP/Postal Code
60153
Country
United States
Facility Name
University of Iowa College of Medicine
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Johns Hopkins School of Medicine
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
Facility Name
University of North Carolina at Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599-7590
Country
United States
Facility Name
Magee-Womens Hospital
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213-3180
Country
United States
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16611949
Citation
Brubaker L, Cundiff GW, Fine P, Nygaard I, Richter HE, Visco AG, Zyczynski H, Brown MB, Weber AM; Pelvic Floor Disorders Network. Abdominal sacrocolpopexy with Burch colposuspension to reduce urinary stress incontinence. N Engl J Med. 2006 Apr 13;354(15):1557-66. doi: 10.1056/NEJMoa054208. Erratum In: N Engl J Med. 2016 Jun 9;374(23):2297-8.
Results Reference
result
PubMed Identifier
18060965
Citation
Burgio KL, Nygaard IE, Richter HE, Brubaker L, Gutman RE, Leng W, Wei J, Weber AM; Pelvic Floor Disorders Network. Bladder symptoms 1 year after abdominal sacrocolpopexy with and without Burch colposuspension in women without preoperative stress incontinence symptoms. Am J Obstet Gynecol. 2007 Dec;197(6):647.e1-6. doi: 10.1016/j.ajog.2007.08.048.
Results Reference
result
PubMed Identifier
18060963
Citation
Bradley CS, Nygaard IE, Brown MB, Gutman RE, Kenton KS, Whitehead WE, Goode PS, Wren PA, Ghetti C, Weber AM; Pelvic Floor Disorders Network. Bowel symptoms in women 1 year after sacrocolpopexy. Am J Obstet Gynecol. 2007 Dec;197(6):642.e1-8. doi: 10.1016/j.ajog.2007.08.023.
Results Reference
result
PubMed Identifier
18185903
Citation
Visco AG, Brubaker L, Nygaard I, Richter HE, Cundiff G, Fine P, Zyczynski H, Brown MB, Weber AM; Pelvic Floor Disorders Network. The role of preoperative urodynamic testing in stress-continent women undergoing sacrocolpopexy: the Colpopexy and Urinary Reduction Efforts (CARE) randomized surgical trial. Int Urogynecol J Pelvic Floor Dysfunct. 2008 May;19(5):607-14. doi: 10.1007/s00192-007-0498-2. Epub 2008 Jan 9.
Results Reference
result
PubMed Identifier
18455536
Citation
Nygaard I, Handa VL, Brubaker L, Borello-France D, Wei J, Wells E, Goode P; Pelvic Floor Disorders Network. Changes in physical activity after abdominal sacrocolpopexy for advanced pelvic organ prolapse. Am J Obstet Gynecol. 2008 May;198(5):570.e1-5. doi: 10.1016/j.ajog.2008.01.044.
Results Reference
result
PubMed Identifier
18656053
Citation
Wren PA, Janz NK, FitzGerald MP, Barber MD, Burgio KL, Cundiff GW, Nygaard IE, Zyczynski HM, Gao X; Pelvic Floor Disorders Network. Optimism in women undergoing abdominal sacrocolpopexy for pelvic organ prolapse. J Am Coll Surg. 2008 Aug;207(2):240-5. doi: 10.1016/j.jamcollsurg.2008.02.019. Epub 2008 May 12.
Results Reference
result
PubMed Identifier
18722933
Citation
Goode PS, Fitzgerald MP, Richter HE, Whitehead WE, Nygaard I, Wren PA, Zyczynski HM, Cundiff G, Menefee S, Senka JM, Gao X, Weber AM; Pelvic Floor Disorders Network. Enhancing participation of older women in surgical trials. J Am Coll Surg. 2008 Sep;207(3):303-11. doi: 10.1016/j.jamcollsurg.2008.03.012. Epub 2008 May 19.
Results Reference
result
PubMed Identifier
18591307
Citation
Brubaker L, Nygaard I, Richter HE, Visco A, Weber AM, Cundiff GW, Fine P, Ghetti C, Brown MB. Two-year outcomes after sacrocolpopexy with and without burch to prevent stress urinary incontinence. Obstet Gynecol. 2008 Jul;112(1):49-55. doi: 10.1097/AOG.0b013e3181778d2a. Erratum In: Obstet Gynecol. 2016 May;127(5):968-969.
Results Reference
result
PubMed Identifier
18976976
Citation
Cundiff GW, Varner E, Visco AG, Zyczynski HM, Nager CW, Norton PA, Schaffer J, Brown MB, Brubaker L; Pelvic Floor Disorders Network. Risk factors for mesh/suture erosion following sacral colpopexy. Am J Obstet Gynecol. 2008 Dec;199(6):688.e1-5. doi: 10.1016/j.ajog.2008.07.029. Epub 2008 Oct 31.
Results Reference
result
PubMed Identifier
18845288
Citation
Bradley CS, Kenton KS, Richter HE, Gao X, Zyczynski HM, Weber AM, Nygaard IE; Pelvic Floor Disorders Network. Obesity and outcomes after sacrocolpopexy. Am J Obstet Gynecol. 2008 Dec;199(6):690.e1-8. doi: 10.1016/j.ajog.2008.07.030. Epub 2008 Oct 9.
Results Reference
result
PubMed Identifier
19701041
Citation
Barber MD, Brubaker L, Nygaard I, Wheeler TL 2nd, Schaffer J, Chen Z, Spino C; Pelvic Floor Disorders Network. Defining success after surgery for pelvic organ prolapse. Obstet Gynecol. 2009 Sep;114(3):600-609. doi: 10.1097/AOG.0b013e3181b2b1ae.
Results Reference
result
PubMed Identifier
32769645
Citation
Lukacz ES, Sridhar A, Chermansky CJ, Rahn DD, Harvie HS, Gantz MG, Varner RE, Korbly NB, Mazloomdoost D; Eunice Kennedy Shriver National Institute of Child Health and Human Development Pelvic Floor Disorders Network (PFDN). Sexual Activity and Dyspareunia 1 Year After Surgical Repair of Pelvic Organ Prolapse. Obstet Gynecol. 2020 Sep;136(3):492-500. doi: 10.1097/AOG.0000000000003992.
Results Reference
derived
PubMed Identifier
21344495
Citation
Barber MD, Chen Z, Lukacz E, Markland A, Wai C, Brubaker L, Nygaard I, Weidner A, Janz NK, Spino C. Further validation of the short form versions of the Pelvic Floor Distress Inventory (PFDI) and Pelvic Floor Impact Questionnaire (PFIQ). Neurourol Urodyn. 2011 Apr;30(4):541-6. doi: 10.1002/nau.20934. Epub 2011 Feb 22.
Results Reference
derived
Links:
URL
http://www.pfdnetwork.org
Description
Pelvic Floor Disorders Network website

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Colpopexy and Urinary Reduction Efforts (CARE) Protocol

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