Clinical trialNCT01272284CompletedInterventional

The Altis® Single Incision Sling System for Female Stress Urinary Incontinence Study

SponsorColoplast A/SEnrollment113Stress Urinary Incontinence

View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

An international, multi-center, single arm, prospective clinical study designed to assess the safety and efficacy of the Coloplast Altis single incision sling system for females with stress urinary incontinence (SUI).

clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

Ervin Kocjancic, MD
University of Chicago, Chicago, IL, United States
Principal Investigator
clinicaltrials.gov ↗

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

17 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada

Chus Hopital Fleurimont
Sherbrooke, Quebec, Canada

United States

Tri Valley Urology
Murrieta, California, United States
Urology Specialists, Llc
Hialeah, Florida, United States
Atlanta Medial Research Institute
Alpharetta, Georgia, United States
Rosemark Womencare Specialist
Idaho Falls, Idaho, United States
University of Illinois at Chicago - Department of Urology
Chicago, Illinois, United States
Illinois Urogynecology, Ltd
Oak Lawn, Illinois, United States
Female Pelvic Medicine & Urogynecology Institute of Michigan
Grand Rapids, Michigan, United States
Bellevue Obgyn
Bellevue, Nebraska, United States
Delaware Valley Urology
Voorhees Township, New Jersey, United States
Carolina Urology Partners
Gastonia, North Carolina, United States
the University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States
Greenville Hospital System
Greenville, South Carolina, United States
Carolina Urologic Research Center
Myrtle Beach, South Carolina, United States
Eastern Virginia Medical School
Norfolk, Virginia, United States
the Group for Women
Norfolk, Virginia, United States
Johnston Willis Medical Center
Richmond, Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start: 31 Dec 2010
Primary completion: 31 Jul 2012
Completion: 31 Jan 2014
Last update posted: 11 Feb 2021
Registered enrollment: 113
Registry id: NCT01272284

clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.