Trial of Percutaneous Tibial Nerve Stimulation (PTNS) Versus PTNS and Fesoterodine Fumarate

PHASE4TerminatedINTERVENTIONAL
Enrollment

4

Participants

Timeline

Start Date

June 30, 2012

Primary Completion Date

March 31, 2013

Study Completion Date

March 31, 2013

Conditions
Overactive Bladder
Interventions
DRUG

Fesoterodine fumarate

PTNS + 4mg of fesoterodine fumarate for 12 weeks

DRUG

Placebo

PTNS + placebo for 12 weeks

PROCEDURE

Percutaneous Tibial Nerve Stimulation (PTNS)

PTNS is an FDA-approved procedure for the diagnosis of overactive bladder, given on a weekly basis. Participants will be given PTNS + either 4mg of fesoterodine fumarate or placebo for 12 weeks, and followed by 4 weeks of washout followed by 12 weeks of PTNS + the opposite treatment (placebo or fesoterodine fumarate).

Trial Locations (1)

85054

Mayo Clinic in Arizona (MCSB and MCH), Phoenix

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Mayo Clinic

OTHER