Non-inferiority of Short-term Catheterization Following Fistula Repair Surgery
Primary Purpose
Vaginal Fistula
Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
7-day catheterization following fistula repair surgery
14 day catheterization
Sponsored by
About this trial
This is an interventional treatment trial for Vaginal Fistula focused on measuring fistula, catheter, surgery, obstetrics, gynecology, urology
Eligibility Criteria
Inclusion Criteria:
- Have a "simple" fistula, as determined at the end of fistula repair surgery (irrespective of the number of prior repair attempts and the cause of the fistula, with the exceptions noted under the exclusion criteria below)
- Have a closed fistula at completion of surgery
- Have a closed fistula 7 days after surgery (i.e. at the time of randomization)
- Understand study procedures and requirements
- Agree to return to the facility for one follow-up visit three month after the date of surgery
- Provide informed consent to participate in the study or in the case of non-emancipated minors, both consent to the study and receive proxy consent to participate in the study
- Have no contraindications precluding their participation.
Exclusion Criteria:
- Have a fistula that is determined to be "not simple" (i.e. intermediate or complex)
- Have a fistula that is radiation-induced, associated with cancer or due to lymphogranuloma venereum (These cases will be excluded because the healing process is very different from fistula resulting from other causes. We expect there to be few cases of these fistulas at the study sites)
- Have a fistula that is not closed immediately after surgery or 7 days after surgery (i.e. at the time of randomization)
Sites / Locations
- Hôpital Saint Joseph
- Gondar University Hospital
- L'Hôpital Préfectoral de Kissidougou
- Kenyatta National Hospital
- National Obstetric Fistula Centre
- Maternité Centrale de Zinder
- Aberdeen Women's Centre
- Kagando Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
7-day catheterization
14-day catheterization
Arm Description
Outcomes
Primary Outcome Measures
Fistula repair breakdown three months following fistula repair surgery as assessed by a urinary dye test.
Secondary Outcome Measures
Repair breakdown one week following catheter removal
Intermittent catheterization due to urinary retention
Prolonged hospitalization
Catheter blockage
Self-reported residual incontinence
The occurrence of septic or febrile episodes
Full Information
NCT ID
NCT01428830
First Posted
September 2, 2011
Last Updated
January 15, 2015
Sponsor
EngenderHealth
Collaborators
World Health Organization, United States Agency for International Development (USAID)
1. Study Identification
Unique Protocol Identification Number
NCT01428830
Brief Title
Non-inferiority of Short-term Catheterization Following Fistula Repair Surgery
Official Title
Non-inferiority of Short-term Catheterization Following Fistula Repair Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
August 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
EngenderHealth
Collaborators
World Health Organization, United States Agency for International Development (USAID)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This facility-based, multi-center randomized controlled trial (RCT) will test the non-inferiority of short-term (7 day) urethral catheterization compared to longer-term (14 day) urethral catheterization in terms of predicting fistula repair breakdown three months following urinary fistula repair surgery. The study will be conducted among 507 women with simple fistula presenting at 8 study sites in Sub-Saharan Africa for fistula repair surgery.
Detailed Description
A vaginal fistula is a devastating condition, affecting an estimated 2 million girls and women across Africa and Asia. Finding ways of providing services in a more efficient and cost-effective manner, without compromising surgical outcomes and the overall health of the patient, is paramount. Shortening the duration of urethral catheterization following fistula repair surgery would increase treatment capacity (by freeing available bed space and increasing availability of nursing staff), lower costs of services, and potentially lower risk of healthcare-associated infections among fistula patients. There is a lack of empirical evidence supporting any particular length of time for urethral catheterization following fistula repair surgery.
This facility-based, multi-center randomized controlled trial (RCT) will test the non-inferiority of short-term (7 day) urethral catheterization compared to longer-term (14 day) urethral catheterization in terms of predicting fistula repair breakdown. The primary outcome is fistula repair breakdown three months following fistula repair surgery as assessed by a urinary dye test, a routine practice in fistula repair services. t. Secondary outcomes will include repair breakdown one week following catheter removal, intermittent catheterization due to urinary retention and the occurrence of septic or febrile episodes, prolonged hospitalization (defined as a stay at the facility beyond one week following initial catheter removal related to an adverse event), catheter blockage, and self-reported residual incontinence. This study will be conducted among 507 women with simple fistula presenting at 8 study sites for fistula repair surgery over the course of 16-18 months at each site.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vaginal Fistula
Keywords
fistula, catheter, surgery, obstetrics, gynecology, urology
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
524 (Actual)
8. Arms, Groups, and Interventions
Arm Title
7-day catheterization
Arm Type
Experimental
Arm Title
14-day catheterization
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
7-day catheterization following fistula repair surgery
Intervention Description
This group will have an indwelling urethral catheter for 7 days following fistula repair surgery.
Intervention Type
Procedure
Intervention Name(s)
14 day catheterization
Intervention Description
This group will have an indwelling urethral catheter for 14 days following fistula repair surgery.
Primary Outcome Measure Information:
Title
Fistula repair breakdown three months following fistula repair surgery as assessed by a urinary dye test.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Repair breakdown one week following catheter removal
Time Frame
14 days or 21 days post-repair
Title
Intermittent catheterization due to urinary retention
Time Frame
7 or 14 days post repair
Title
Prolonged hospitalization
Time Frame
14 or 21 days post-repair
Title
Catheter blockage
Time Frame
14 or 21 days post repair
Title
Self-reported residual incontinence
Time Frame
3 months
Title
The occurrence of septic or febrile episodes
Time Frame
14 or 21 days post-repair
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Have a "simple" fistula, as determined at the end of fistula repair surgery (irrespective of the number of prior repair attempts and the cause of the fistula, with the exceptions noted under the exclusion criteria below)
Have a closed fistula at completion of surgery
Have a closed fistula 7 days after surgery (i.e. at the time of randomization)
Understand study procedures and requirements
Agree to return to the facility for one follow-up visit three month after the date of surgery
Provide informed consent to participate in the study or in the case of non-emancipated minors, both consent to the study and receive proxy consent to participate in the study
Have no contraindications precluding their participation.
Exclusion Criteria:
Have a fistula that is determined to be "not simple" (i.e. intermediate or complex)
Have a fistula that is radiation-induced, associated with cancer or due to lymphogranuloma venereum (These cases will be excluded because the healing process is very different from fistula resulting from other causes. We expect there to be few cases of these fistulas at the study sites)
Have a fistula that is not closed immediately after surgery or 7 days after surgery (i.e. at the time of randomization)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark A Barone, DVM, MS
Organizational Affiliation
EngenderHealth
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mariana Widmer
Organizational Affiliation
World Health Organization
Official's Role
Study Director
Facility Information:
Facility Name
Hôpital Saint Joseph
City
Kinshasa
Country
Congo, The Democratic Republic of the
Facility Name
Gondar University Hospital
City
Gondar
Country
Ethiopia
Facility Name
L'Hôpital Préfectoral de Kissidougou
City
Kissidougou
Country
Guinea
Facility Name
Kenyatta National Hospital
City
Nairobi
Country
Kenya
Facility Name
National Obstetric Fistula Centre
City
Abakaliki
Country
Nigeria
Facility Name
Maternité Centrale de Zinder
City
Zinder
Country
Niger
Facility Name
Aberdeen Women's Centre
City
Freetown
Country
Sierra Leone
Facility Name
Kagando Hospital
City
Kasese District
Country
Uganda
12. IPD Sharing Statement
Citations:
PubMed Identifier
25911172
Citation
Barone MA, Widmer M, Arrowsmith S, Ruminjo J, Seuc A, Landry E, Barry TH, Danladi D, Djangnikpo L, Gbawuru-Mansaray T, Harou I, Lewis A, Muleta M, Nembunzu D, Olupot R, Sunday-Adeoye I, Wakasiaka WK, Landoulsi S, Delamou A, Were L, Frajzyngier V, Beattie K, Gulmezoglu AM. Breakdown of simple female genital fistula repair after 7 day versus 14 day postoperative bladder catheterisation: a randomised, controlled, open-label, non-inferiority trial. Lancet. 2015 Jul 4;386(9988):56-62. doi: 10.1016/S0140-6736(14)62337-0. Epub 2015 Apr 21.
Results Reference
derived
PubMed Identifier
22433581
Citation
Barone MA, Frajzyngier V, Arrowsmith S, Ruminjo J, Seuc A, Landry E, Beattie K, Barry TH, Lewis A, Muleta M, Nembunzu D, Olupot R, Sunday-Adeoye I, Wakasiaka WK, Widmer M, Gulmezoglu AM. Non-inferiority of short-term urethral catheterization following fistula repair surgery: study protocol for a randomized controlled trial. BMC Womens Health. 2012 Mar 20;12:5. doi: 10.1186/1472-6874-12-5.
Results Reference
derived
Learn more about this trial
Non-inferiority of Short-term Catheterization Following Fistula Repair Surgery
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