Actively Recruiting
Effectiveness of Pelvic Floor Therapy for the Management of Erectile Dysfunction and Premature Ejaculation.
Led by Boston Medical Group · Updated on 2026-01-23
66
Participants Needed
1
Research Sites
265 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this clinical trial is to evaluate the effectiveness of pelvic floor therapy for the management of erectile dysfunction and premature ejaculation in patients with erectile dysfunction and premature ejaculation. The main question to answer is: What is the effectiveness of pelvic floor therapy (electrostimulation, biofeedback, and therapeutic exercise) for the treatment of patients with erectile dysfunction and or premature ejaculation? Patients will: * Have an initial consultation of pelvic floor rehabilitation before therapy. * Be given pelvic floor therapy. * Have a secondary consultation of pelvic floor rehabilitation after therapy. Three intervention groups will be included: Group 1: Patients with premature ejaculation Group 2: Patients with erectile dysfunction Group 3: Patients with erectile dysfunction and premature ejaculation.
CONDITIONS
Official Title
Effectiveness of Pelvic Floor Therapy for the Management of Erectile Dysfunction and Premature Ejaculation.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male participants aged over 18 years
- Erectile dysfunction or premature ejaculation lasting at least 6 months
- Sexual activity with a heterosexual partner at least once a week
- Signed informed consent before starting the study
- For premature ejaculation group: Premature ejaculation diagnosis by ISSM criteria
- Premature Ejaculation Diagnosis Tool (PEDT) score greater than 11
- For erectile dysfunction group: Clinical diagnosis of primary erectile dysfunction
- International Index Erectile Function - Erectile Function domain (IIEF-EF) score less than 26
You will not qualify if you...
- Pharmacological treatment for erectile dysfunction or premature ejaculation in the last 3 months
- Erection Hardness Score greater than 3 for erectile dysfunction patients
- History or suspicion of hypogonadism with Aging Males Symptoms (AMS) score greater than 36 for erectile dysfunction patients
- History of pelvic radiotherapy
- Presence of pacemaker, cardiac arrhythmia, or epilepsy
- History of spinal cord trauma or spinal surgeries
- Inability to attend therapies or follow-up visits
- Illiteracy or cognitive disability preventing questionnaire completion
- Psychiatric, psychological disorders, or cognitive deficiencies
- Injuries in the therapy application area
- Active pelvic organ cancer
AI-Screening
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Trial Site Locations
Total: 1 location
1
Boston Medical Group Colombia
Bogotá, Cundinamarca, Colombia, 11022
Actively Recruiting
Research Team
C
Carolina Sandoval, Master
CONTACT
H
Héctor Corredor, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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