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

NACompletedINTERVENTIONAL
Enrollment

113

Participants

Timeline

Start Date

December 31, 2010

Primary Completion Date

July 31, 2012

Study Completion Date

January 31, 2014

Conditions
Stress Urinary Incontinence
Interventions
DEVICE

Altis® Single Incision Sling System (SIS)

The Altis® SIS is a permanently implantable synthetic sling for females placed at the mid-urethra to provide a scaffold for tissue in-growth and support for stress urinary incontinence.

Trial Locations (17)

23235

Johnston Willis Medical Center, Richmond

23502

The Group for Women, Norfolk

23507

Eastern Virginia Medical School, Norfolk

28054

Carolina Urology Partners, Gastonia

29572

Carolina Urologic Research Center, Myrtle Beach

29605

Greenville Hospital System, Greenville

30005

Atlanta Medial Research Institute, Alpharetta

33016

Urology Specialists, LLC, Hialeah

49503

Female Pelvic Medicine & Urogynecology Institute of Michigan, Grand Rapids

60453

Illinois Urogynecology, LTD, Oak Lawn

60612

University of Illinois at Chicago - Department of Urology, Chicago

68123

Bellevue ObGyn, Bellevue

73104

The University of Oklahoma Health Sciences Center, Oklahoma City

83404

Rosemark Womencare Specialist, Idaho Falls

92562

Tri Valley Urology, Murrieta

08043

Delaware Valley Urology, Voorhees Township

J1H 5N4

CHUS Hopital Fleurimont, Sherbrooke

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Coloplast A/S

INDUSTRY

NCT01272284 - The Altis® Single Incision Sling System for Female Stress Urinary Incontinence Study | Biotech Hunter | Biotech Hunter