Control of urinary loss in men undergoing prostate surgery

Phase 2

• Conditions: rinary incontinence; Urinary Incontinence, Urge; Urinary Incontinence, Stress; Prostatic Neoplasms; C12.777.934.852; C12.777.934.852.500; C12.777.934.852.249; C04.588.945.440.770

• Registration Number: RBR-3jm5y2
• Lead Sponsor: niversidade Federal de Minas Gerais

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-07-24
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Male
• Target Recruitment: Not specified

Inclusion Criteria

Preserved locomotor, visual, auditory and swallowing capacity; Have a preserved cognitive function, verified by means of a six-item cognitive impairment test; Present urinary incontinence with the need to use at least one or more absorbents daily; Have a loss greater than one gram assessed using the Pad Test; Have removed the delayed bladder catheter within 10 to 15 days

Exclusion Criteria

Do not respond to three attempts at contact made by the researcher; Need for readmission; Be in chemotherapy or radiotherapy treatment; Presence of rectum urethral fistula; Presence of urinary incontinence before the surgical procedure; Urinary tract infection (UTI), with urine culture test showing multi-resistant bacteria and more than one cycle of antibiotic therapy; Infection, inflammation or injury to the ear; Allergy to metal or micropore; Not having financial conditions and availability to be at the place of the study; Use of other complementary therapies up to three months prior to the study

Study & Design

• Study Type: Intervention
• Study Design: Not specified