The Altis® Single Incision Sling System for Female Stress Urinary Incontinence Study
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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
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
Conditions
Interventions
- Altis® Single Incision Sling System (SIS) Device
Device
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
- Nov 30, 2010
- Primary completion
- Jun 30, 2012
- Completion
- Dec 31, 2013
- Last update posted
- Feb 10, 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 10, 2021 · Synced Jul 21, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01272284 live on ClinicalTrials.gov.