Study to Evaluate NVC-422 for Urinary Catheter Blockage and Encrustation

PHASE2CompletedINTERVENTIONAL
Enrollment

67

Participants

Timeline

Start Date

November 30, 2010

Primary Completion Date

July 31, 2013

Study Completion Date

August 31, 2013

Conditions
Urinary Catheter Blockage and Encrustation
Interventions
DRUG

NVC-422, 0.2%

0.2% NVC-422 (sterile), 25 ml instilled and retained in catheter for 15 min, 2x/day; 8 treatments administered over a 26 day period

DRUG

Sterile normal saline, 0.9%

Saline (sterile), 25 ml instilled and retained in catheter for 15 min, 2x/day; 8 treatments administered over a 26 day period

Trial Locations (8)

19107

Thomas Jefferson University, Philadelphia

23249

McGuire Veterans Affairs Medical Center, Richmond

28203

Carolinas Medical Center, Charlotte

29572

Carolina Urologic Research Center, Myrtle Beach

34102

Specialists in Urology, Naples

90242

Los Amigos Research and Education Institute (LAREI), Downey

98043

Integrity Medical Research, Mountlake Terrace

07052

Kessler Institute for Rehabilitation, West Orange

Sponsors
All Listed Sponsors
lead

NovaBay Pharmaceuticals, Inc.

INDUSTRY

NCT01243125 - Study to Evaluate NVC-422 for Urinary Catheter Blockage and Encrustation | Biotech Hunter | Biotech Hunter