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Trial of Small Intestine Submucosa (SIS) Mesh for Anterior Repair: A Pilot Study

Randomized Controlled Trial of SIS Mesh for Anterior Repair: A Pilot Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00955448
Acronym
Anterior SIS
Enrollment
57
Registered
2009-08-10
Start date
2009-12-31
Completion date
2012-04-30
Last updated
2016-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Pelvic Organ Prolapse

Keywords

Anterior pelvic organ prolapse, Surgical repair, Pelvic floor surgery, Randomized clinical trial

Brief summary

Prolapse occurs when pelvic organs drop down and cause a bulging of the tissues. An anterior wall prolapse occurs when the front of the vagina loses its support, and the bladder drops down and rotates into the vaginal opening. The bladder can cause a bulge out of the vagina. One of the treatment options available is to repair the anterior wall surgically. The goals of surgery are to return the anatomy to its usual position, ensuring that all the pelvic floor organs (bladder, vagina and rectum) can function properly. The ideal surgical repair would also be long lasting. Two surgical options are routinely performed in Calgary for repair of an anterior compartment prolapse. One option involves fixing the organs back in place using sutures. The other option uses sutures plus a mesh made of small intestine submucosa (SIS) that is already licensed for use in Canada. The SIS mesh is slowly absorbed after it is placed in the pelvic area. The investigators do not know which of these two options is the best surgical procedure. Both may have different advantages that would result in better results. This study is designed to try and find out if one of these procedures is better, and if a larger study may be needed.

Interventions

DEVICESIS mesh (Cook Medical)

Anterior prolapse repair will be reinforced using surgical mesh made from porcine small intestine mucosa (Cook Medical)

PROCEDUREAnterior prolapse repair

Anterior prolapse repair will be conducted without using mesh reinforcement

Sponsors

Cook Group Incorporated
CollaboratorINDUSTRY
Alberta Health services
CollaboratorOTHER
University of Calgary
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Women who require surgical correction for anterior compartment prolapse. (Concomitant surgery is permitted.) * Point Ba of 0 or greater: that is a positive Ba, indicating that the prolapse is beyond the introitus, not within the vagina. * Patient must consent to participate in the study.

Exclusion criteria

* Having an obliterative procedure (Lefort procedure or colpocleisis). * Allergy to graft material. * Immunocompromised. * Previous anterior compartment repair. * Are unable to understand English. * Will be unavailable for follow-up.

Design outcomes

Primary

MeasureTime frame
Objective assessment of prolapse. Cure is defined as point Ba (on POP-Q) of -1 or above (i.e., more negative)12 months postoperatively

Secondary

MeasureTime frame
Pelvic Organ Prolapse Quantification(POP-Q) stage12 months postoperatively
Change in POP-Q stage from baseline12 months postoperatively
Postoperative complications12 months postoperatively
Pelvic Floor Distress Inventory short form-20 (PFDI-20)12 months postoperatively
Change in point Ba (on POP-Q) from baseline12 months postoperatively
Sexual function (Pelvic Organ Prolapse/Urinary Incontinence Sexual Function Questionnaire (PISQ-12)12 months postoperatively
Surgical complicationsUp to 6 weeks postoperatively
Satisfaction with surgical outcome12 months postoperatively
Pelvic Floor Impact Questionnaire short form-7 (PFIQ-7)12 months postoperatively

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026