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A Sham Controlled Study of the Effects of Ultrasonic Shockwaves as a Treatment for Chronic Pelvic Pain (CPPESWT)

Primary Purpose

Chronic Pelvic Pain

Status
Withdrawn
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Low intensity extracorporeal shockwave therapy
Sham low intensity extracorporeal shockwave therapy
Sponsored by
Herlev Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pelvic Pain focused on measuring ESWT, Chronic pelvic pain, randomized, sham controlled

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • pelvic pain with a duration of more than 6 months
  • be able to read and understand the study information

Exclusion Criteria:

  • known etiology for pelvic pain eg. cancer, infection, inherent abnormalities.
  • diagnosed with hemophilia
  • receiving anti thrombotic therapy other than hearth magnyl
  • diagnosed with thrombocytosis
  • active cancer
  • treated with IV glucocorticoids within the last 6 months
  • disease in the rectal area
  • abnormal digital rectal exploration
  • bacteriospermia

Sites / Locations

  • Birthe bonde klinikken

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Low intensity extracorporeal shockwave therapy

Sham low intensity extracorporeal shockwave therapy

Arm Description

Active treatment with low intensity extracorporeal shockwave therapy applied to the perineum.

Sham treatment with low intensity extracorporeal shockwave therapy applied to the perineum.

Outcomes

Primary Outcome Measures

Change in NIH-Chronic Prostatitis Symptom Index
A questionnaire designed to provide symptom scores for patients with chronic prostatitis. The index provides scores on pain, urinary symptoms, and quality of life.

Secondary Outcome Measures

Change in The International Index of Erectile Function 5
Questionnaire designed to evaluate erectile capabilities. The questionnaire provides a score between 5 and 25.
Change in The International prostate symptom score
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
One question designed to estimate treatment satisfaction on a four point Likert scale.

Full Information

First Posted
January 10, 2014
Last Updated
March 23, 2015
Sponsor
Herlev Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02042651
Brief Title
A Sham Controlled Study of the Effects of Ultrasonic Shockwaves as a Treatment for Chronic Pelvic Pain
Acronym
CPPESWT
Official Title
Low Intensity Extracorporeal Shockwave Therapy Against Chronic Pelvic Pain: a Randomized and Sham Controled Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Withdrawn
Why Stopped
study stopped because of insuficient number of comparable patients available.
Study Start Date
February 2014 (undefined)
Primary Completion Date
February 2016 (Anticipated)
Study Completion Date
February 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Herlev Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Introduction: 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. Methods: 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pelvic Pain
Keywords
ESWT, Chronic pelvic pain, randomized, sham controlled

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Low intensity extracorporeal shockwave therapy
Arm Type
Experimental
Arm Description
Active treatment with low intensity extracorporeal shockwave therapy applied to the perineum.
Arm Title
Sham low intensity extracorporeal shockwave therapy
Arm Type
Sham Comparator
Arm Description
Sham treatment with low intensity extracorporeal shockwave therapy applied to the perineum.
Intervention Type
Device
Intervention Name(s)
Low intensity extracorporeal shockwave therapy
Other Intervention Name(s)
Storz Duolith® SD1 T-TOP, CE 1275
Intervention Description
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
Intervention Type
Device
Intervention Name(s)
Sham low intensity extracorporeal shockwave therapy
Other Intervention Name(s)
Storz Duolith® SD1 T-TOP, CE 1275
Intervention Description
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.
Primary Outcome Measure Information:
Title
Change in NIH-Chronic Prostatitis Symptom Index
Description
A questionnaire designed to provide symptom scores for patients with chronic prostatitis. The index provides scores on pain, urinary symptoms, and quality of life.
Time Frame
Change from baseline to twelve weeks after final treatment
Secondary Outcome Measure Information:
Title
Change in The International Index of Erectile Function 5
Description
Questionnaire designed to evaluate erectile capabilities. The questionnaire provides a score between 5 and 25.
Time Frame
Change from baseline to twelve weeks after final treatment
Title
Change in The International prostate symptom score
Description
A questionnaire designed to provide information on lower urinary tract symptoms and their impact on quality of life. scores range from 0 to 35.
Time Frame
Change from baseline to twelve weeks after final treatment
Title
Global satisfaction score
Description
One question designed to estimate treatment satisfaction on a four point Likert scale.
Time Frame
Twelve weeks after final treatment

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: pelvic pain with a duration of more than 6 months be able to read and understand the study information Exclusion Criteria: known etiology for pelvic pain eg. cancer, infection, inherent abnormalities. diagnosed with hemophilia receiving anti thrombotic therapy other than hearth magnyl diagnosed with thrombocytosis active cancer treated with IV glucocorticoids within the last 6 months disease in the rectal area abnormal digital rectal exploration bacteriospermia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anders U Frey, Bach. Med.
Organizational Affiliation
Urological Research Unit, Herlev Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Birthe bonde klinikken
City
Copenhagen E
State/Province
Copenhagen
ZIP/Postal Code
2100
Country
Denmark

12. IPD Sharing Statement

Learn more about this trial

A Sham Controlled Study of the Effects of Ultrasonic Shockwaves as a Treatment for Chronic Pelvic Pain

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