TECAR Therapy on Pain and Quality of Life in Men With Chronic Prostatitis/Chronic Pelvic Pain Syndrome

ConditionProstatitis
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age30-50
SponsorMiddle East University

About this trial

Evaluate the effect of TECAR therapy on pain, voiding, erectile function, sleep quality and quality of life in men with chronic prostatitis/chronic pelvic pain syndrome.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Presence of chronic prostatitis/chronic pelvic pain symptoms for more than 6 months.

Ages will be ranged from 30 to 50 years old.

Disqualifiers

Urinary and seminal infections.

Recent parenteral steroid administration.

Prior prostate or pelvic surgery.

Lower urinary tract disorders such as bladder stones.

Trial design

Design model

Parallel

Treatments tested in this trial

  • TECAR therapy

    Device

    WINBACK 3SE (France) will be used for TECAR therapy in this study. To facilitate optimal distribution of endogenous heat therapy and effective contact between the active electrodes, both capacitive and resistive, and the surface of the skin, a layer of high-conductivity cream will be applied to the treatment region. The plate, an inactive electrode, which has a specific size (21cm\*15cm), will be placed on the gluteal region. The capacitive electrode was employed for a duration of seven and a half minutes, at an intensity of 30-40%, whereas the resistance electrode will be utilized for an equivalent period over the perineum at the same intensity.

  • Sham TECAR therapy

    Device

    The procedure is similar to the active treatment of TECAR, but with the critical difference being that the output intensity of the TECAR device will be set to zero during the session.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: TECAR therapy groupActive comparator 1 intervention
Group B: Control groupSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pelvic pain

Pain will be assessed using the National Institutes of Health-Chronic Prostatitis Symptom Index

Time frame
Baseline and 8 weeks later

Secondary outcomes

1

Quality of life of men

Quality of life will be assessed using the National Institutes of Health-Chronic Prostatitis Symptom Index

Time frame
Baseline and after 8 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: