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Completed Not applicable Interventional Results available

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

ClinicalTrials.gov ID: NCT01272284

Public ClinicalTrials.gov record NCT01272284. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 6:18 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT01272284
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Coloplast A/S
Industry
Enrollment
113 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2010 (Type not available)
Primary completion
Jul 2012 (Actual)
Completion
Jan 2014 (Actual)
Last update posted
Feb 11, 2021

2010 – 2014

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Tri Valley Urology Murrieta California 92562 —
Urology Specialists, LLC Hialeah Florida 33016 —
Atlanta Medial Research Institute Alpharetta Georgia 30005 —
Rosemark Womencare Specialist Idaho Falls Idaho 83404 —
University of Illinois at Chicago - Department of Urology Chicago Illinois 60612 —
Illinois Urogynecology, LTD Oak Lawn Illinois 60453 —
Female Pelvic Medicine & Urogynecology Institute of Michigan Grand Rapids Michigan 49503 —
Bellevue ObGyn Bellevue Nebraska 68123 —
Delaware Valley Urology Voorhees Township New Jersey 08043 —
Carolina Urology Partners Gastonia North Carolina 28054 —
The University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Greenville Hospital System Greenville South Carolina 29605 —
Carolina Urologic Research Center Myrtle Beach South Carolina 29572 —
The Group for Women Norfolk Virginia 23502 —
Eastern Virginia Medical School Norfolk Virginia 23507 —
Johnston Willis Medical Center Richmond Virginia 23235 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01272284, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 11, 2021 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01272284 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →