A Sham Controlled Study of the Effects of Ultrasonic Shockwaves as a Treatment for Chronic Pelvic Pain (CPPESWT)
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|ClinicalTrials.gov Identifier: NCT02042651|
Recruitment Status : Withdrawn (study stopped because of insuficient number of comparable patients available.)
First Posted : January 23, 2014
Last Update Posted : March 24, 2015
Chronic pelvic pain with unknown pathology is a condition that affects both men and women. the condition is defined as pelvic pain lasting for a minimum of 6 months without any known etiology eg. cancer, infection or inherent anatomical abnormalities. Low intensity extracorporeal shockwave therapy (LIESWT) enables the practitioner to deliver a small amount of energy approximately 5 cm under the skin of the patient without damaging the skin. This have been shown to increase blood flow and accelerate healing which could also be beneficial in chronic pelvic pain patients.The purpose of this study is to investigate the effects of LIESWT on chronic pelvic pain.
All patients will be treated at the Birthe Bonde clinic, in Copenhagen, Denmark.
The investigators anticipate to include 100 chronic pelvic pain patients in the study.
included patients will be randomized into two groups: active treatment or sham treatment.
All patients will be required to provide a urine sample and a semen sample prior to final inclusion. Samples will be analyzed for microbial growth. Furthermore, patients will undergo a digital rectal exploration and finally all patients is required to provide an informed consent in order to be included in the study.
A Storz Doulith SD1 T-Top (CE1275) will be used to generate shockwaves. Patients will receive the treatment once a week until their symptoms have seized or for a maximum of 6 times. Each treatment consists of 3000 shockwaves applied to the perineum with a energy density of 0.25-0.40 millijoule(mJ)/mm2 and a frequency of 3 hz.
Participants will fill out a questionnaire one week before the treatment, one week, four weeks, and twelve weeks after the last treatment.
Possible gains from this study:
The investigators hope to provide further evidence for this treatment and consequently be able to offer the treatment as an alternative to the very limited array of treatments existing for this group of patients today.
Ethics, funding, and publication:
The study is performed in compliance with the Helsinki declaration. External funding have been applied for but not yet received. Participants will be informed of sources of external funding. The result of the study will be published as soon as possible, preferably in a peer-reviewed international journal.
|Condition or disease||Intervention/treatment||Phase|
|Chronic Pelvic Pain||Device: Low intensity extracorporeal shockwave therapy Device: Sham low intensity extracorporeal shockwave therapy||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Investigator)|
|Official Title:||Low Intensity Extracorporeal Shockwave Therapy Against Chronic Pelvic Pain: a Randomized and Sham Controled Study|
|Study Start Date :||February 2014|
|Estimated Primary Completion Date :||February 2016|
|Estimated Study Completion Date :||February 2016|
Experimental: Low intensity extracorporeal shockwave therapy
Active treatment with low intensity extracorporeal shockwave therapy applied to the perineum.
Device: Low intensity extracorporeal shockwave therapy
Shockwaves will be applied to the perineum a total of 6 times once per week. The energy level applied will range between 0.25 and 0.40 mJ/mm2 with a frequency of 3 Hz for a total of 3000 shockwaves per treatment session
Other Name: Storz Duolith® SD1 T-TOP, CE 1275
Sham Comparator: Sham low intensity extracorporeal shockwave therapy
Sham treatment with low intensity extracorporeal shockwave therapy applied to the perineum.
Device: Sham low intensity extracorporeal shockwave therapy
Shockwaves will be applied to the perineum a total of 6 times once per week. The shockwaves will be blocked by a medium on the handheld applicator.
Other Name: Storz Duolith® SD1 T-TOP, CE 1275
- Change in NIH-Chronic Prostatitis Symptom Index [ Time Frame: Change from baseline to twelve weeks after final treatment ]A questionnaire designed to provide symptom scores for patients with chronic prostatitis. The index provides scores on pain, urinary symptoms, and quality of life.
- Change in The International Index of Erectile Function 5 [ Time Frame: Change from baseline to twelve weeks after final treatment ]Questionnaire designed to evaluate erectile capabilities. The questionnaire provides a score between 5 and 25.
- Change in The International prostate symptom score [ Time Frame: Change from baseline to twelve weeks after final treatment ]A questionnaire designed to provide information on lower urinary tract symptoms and their impact on quality of life. scores range from 0 to 35.
- Global satisfaction score [ Time Frame: Twelve weeks after final treatment ]One question designed to estimate treatment satisfaction on a four point Likert scale.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02042651
|Birthe bonde klinikken|
|Copenhagen E, Copenhagen, Denmark, 2100|
|Principal Investigator:||Anders U Frey, Bach. Med.||Urological Research Unit, Herlev Hospital|