Non-inferiority of Short-term Catheterization Following Fistula Repair Surgery

EngenderHealth

Status

Completed

Conditions

Vaginal Fistula

Treatments

Procedure: 7-day catheterization following fistula repair surgery

Procedure: 14 day catheterization

Study type

Interventional

Funder types

Other

Other U.S. Federal agency

Identifiers

NCT01428830

A65783

Details and patient eligibility

About

Full 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.

Enrollment

524 patients

Sex

Female

Volunteers

No Healthy Volunteers

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)