Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Outcome Measure:

Complete continence (PAD test 24 hours <10 cc)

Outcome Time Frame:

12 months

Safety Issue:

No

Principal Investigator

Carlo Cisari, prof.

Investigator Role:

Study Director

Investigator Affiliation:

AUO "Maggiore della Carità" - Novara

Authority:

Italy: National Monitoring Centre for Clinical Trials - Ministry of Health

Study ID:

NO08974

NCT ID:

NCT00982098

Start Date:

February 2007

Completion Date:

November 2009

Related Keywords:

• Urinary Incontinence
• Prostatectomy
• Prostatic cancer
• Urinary incontinence
• Exercise
• Electric stimulation therapy
• Counseling
• Urinary Incontinence