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Clinical Trials/NCT02226237
NCT02226237
Completed
Not Applicable

URINARY INCONTINENCE AND ERECTIL DYSFUNCTION AFTER RADICAL PROSTATECTOMY: A Randomized Controlled Trial Comparing Pelvic Muscle Exercises With or Without Electrical Stimulation

Barretos Cancer Hospital1 site in 1 country237 target enrollmentSeptember 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Urinary Incontinence
Sponsor
Barretos Cancer Hospital
Enrollment
237
Locations
1
Primary Endpoint
recovery of urinary continence
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The prostate cancer is the most common parenchymal neoplasia in men over 45 years old. Radical prostatectomy is curative treatment is most used today. Urinary incontinence and erectile dysfunction are the main complications of radical prostatectomy. Physical therapy has been used as a form of conservative treatment of these complications. However, the role of physiotherapy in the treatment of these complications is not well defined in the literature. We will do a randomized controlled study with patients undergoing radical prostatectomy. After removal of the Foley catheter, patients will be randomized into 3 groups: control group, group of pelvic floor exercises and anal electrostimulation group. These patients will be evaluated preoperatively in an attempt to meet prognostic factors for urinary incontinence and erectile dysfunction. They will be followed by 2 years after surgery, to assess whether the therapy will alter the course of urinary continence and erectile function in these patients.

Detailed Description

Randomization was performed by a team of external statistics to the research team, using the method of randomization in blocks of three, who were randomly selected. The group to which the patient was allocated to researchers only be informed at the time of randomization, if patients satisfied the criteria for inclusion and exclusion. Will be evaluated preoperatively: urodynamic studies and clinical evaluation. The following clinical data were evaluated: Body Mass Index (BMI), comorbidities, disease staging and sociodemographic information. The following parameters will be evaluated in the pre-operative and after one, three, six and twelve months after surgery: evaluating the strength of the pelvic floor through perineometry, the 1 hour pad test, electromyographic evaluation of pelvic floor, and the application of instruments validated for the Portuguese language. The follow instruments will be applied: International Index of Erectile Function - 5 questions (IIEF-5), International Consultation on Incontinence Questionnaire - Short Form (ICIQ-SF), International Prostate Symptom Score (IPSS).

Registry
clinicaltrials.gov
Start Date
September 2010
End Date
December 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
Barretos Cancer Hospital
Responsible Party
Principal Investigator
Principal Investigator

Wesley Justino Magnabosco

MD

Barretos Cancer Hospital

Eligibility Criteria

Inclusion Criteria

  • patients over 18 years
  • diagnosed with localized or locally advanced prostate cancer
  • that are undergoing radical prostatectomy as treatment of the condition
  • they are coming from Barretos or a nearby region or has logistics facilities to come to the Barretos Cancer Hospital to perform the followup

Exclusion Criteria

  • those with mental or physical problems that make it impossible to collect data or that may influence the recovery of continence postoperatively
  • patients with metastatic prostate cancer
  • patients not undergoing retropubic prostatectomy as treatment for prostate cancer

Outcomes

Primary Outcomes

recovery of urinary continence

Time Frame: one year

recovery of erectile function

Time Frame: two years

Secondary Outcomes

  • evaluate prognosis for recovery of urinary continence(one year)

Study Sites (1)

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