- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00194623
Botox as a Treatment for Chronic Male Pelvic Pain Syndrome
Botox (Botulinum Toxin A) as a Treatment for Chronic Male Pelvic Pain Syndrome: A Randomized Placebo Controlled Trial
Chronic pelvic pain syndrome (CPPS) is thought to affect approximately 8% of men aged 18 and older. Patients with this condition experience pain in the perineum, the genitalia, and the rectum. As well, there is associated voiding, sexual, and ejaculatory dysfunction. The impact of patient well-being is thought to be equivalent to patients with congestive heart failure. The etiology of this condition is unknown, thus making treatment very difficult. Researchers have pursued an infectious cause for the disease; however, studies have failed to substantiate this theory. Despite this, the main treatment offered to patients is long-term antibiotic therapy. Results from this treatment modality have been unsatisfactory.
Other groups have postulated that the symptoms of CPPS may be secondary to neuromuscular factors. Some studies have demonstrated increases in pelvic muscular tone. Maneuvers such as prostate massage and levator massage have shown some benefit in relieving symptoms. Treatment with alpha-blockers to relax prostate smooth muscle has brought about improvement in a portion of patients. Use of generalized muscle relaxants has produced mediocre results.
However, many of these neuromuscular treatments are generalized and do not target the perineal musculature directly. It is theorized that spasm of the perineal muscles triggered by an unknown noxious stimuli (e.g. infection) cause the pain and symptoms of CPPS. At our center, we have performed pilot studies using botulinum toxin A. Four patients were treated with Botox". 100 U were injected in three locations in the midline of the bulbocavernosus muscle. The bulbocavernosus muscle is easily accessible and shares innervation with the pelvic musculature. Patient's response to medication was measured by the NIH Prostatitis pain scale and as well as the University of Washington prostatitis pain scale. All patients reported resolution of symptoms. Remission lasted for duration of 10-12 weeks. No patients reported adverse events.
HYPOTHESIS
Botulinum toxin A is effective in the treatment of chronic pelvic pain syndrome in men.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Visit 1 Patient will review and sign the study consent form. Subject will be asked to complete questionnaires. Then, patient will then be asked to give a semen sample.
Visit 2 (1 week after Visit I) Prior to this visit, the patient will be randomized to either active medication or placebo. First, the patient will then undergo a physical exam including a genital and rectal exam. Then, the patient will be brought in to the room and placed in lithotomy position. The perineum will be prepped with iodine solution. EMG electrodes and a ground will be placed in the perineum. Three landmarks (1. middle of bulbospongiosus muscle; 2. perineal body; 3. an area equidistant from 1 and 2) will be marked using a skin marker. The EMG needle will be placed into each landmark and the patient will be asked to squeeze his perineal muscles. Once in the proper location, 1.3 cc of medication (active drug or placebo) will be distributed into these landmarks. The remaining 2.6 ccs will be injected into 2 other painful pelvic muscle sites as determined physical exam. The area will then be gently massaged.
Month Post Injection Mailing:
The patient will be mailed a packet containing follow-up questionnaires.
- Month Post Injection Mailing: Same as 1 Month Post Injection Visit.
- Month Post Visit (Visit 3) First, the subject will be asked to fill out follow-up questionnaires. Next, a physical exam and prostate massage will be performed and expressed prostatic secretions collected. Finally, the subject will be asked to provide a semen sample.
Optional open label trial for those patients randomized to placebo section:
Open label injection visit (Visit 4) Injection of open label Botox as in Visit 2.
Month Post Open Label Botox Injection Mailing:
The patient will be mailed a packet containing follow-up questionnaires.
Month Post Open Label Botox Injection Mailing:
Same as 1 Month Post Injection mailing.
- Month Post Open Label Injection Visit:
Same as Visit 3.
Study Type
Enrollment
Phase
- Phase 4
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Men aged 18 and older
- History of chronic pelvic pain syndrome (NIH type IIIA and IIIB) for at least 3 months
- No antibiotics or new treatment for prostatitis for at least 30 days
- Written informed consent and written authorization for use or release of health and research study information have been obtained.
- Subject has severity/stage of disease: pain areas must include perineum.
- Laboratory findings required : negative urine cultures.
- Ability to follow study instructions and likely to complete all required visits.
Exclusion Criteria:
- Documented urinary tract infection
- Bacteria isolated to the prostate from segmental urine cultures
- Pain from another source in the genitourinary tract (e.g. renal colic)
- Genitourinary (GU) malignancy
- History of radiation to the GU tract
- Previous or current botulinum therapy
- Known allergy or sensitivity to any study medication (Botox, lidocaine)
- Diagnosis of myasthenia gravis, Eaton-Lambert Syndrome, Amyotrophic Lateral Sclerosis, spinal cord injury or any other significant disease which might interfere with neuromuscular transmission
- Concurrent use of aminoglycoside antibiotics or agents that interfere with neuromuscular transmission
- Profound atrophy or excessive weakness of the muscles to be injected
- Infection at the injection site or systemic infection
- Concurrent participation in another investigational drug study
- Is overtly psychotic or suicidal.
- Has post-surgical pain
- Has back or rectal pain only.
- Was treated for prostate, bladder, renal or other genitourinary malignancy
- Had in the past or is currently undergoing radiation therapy
- Has a history of genitourinary tuberculosis
- Is currently taking antibiotics.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Double
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
NIH-CPSI -pain scores at 3 months post-treatment follow-up
Time Frame: 3 months post treatment
|
3 months post treatment
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
AUA score at 3 months post-treatment follow-up
Time Frame: 3 months post-treatment
|
3 months post-treatment
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Richard E Berger, MD, Professor of Urology
Study record dates
Study Major Dates
Study Start
Study Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Mental Disorders
- Pathologic Processes
- Pain
- Neurologic Manifestations
- Disease
- Syndrome
- Somatoform Disorders
- Pelvic Pain
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Peripheral Nervous System Agents
- Cholinergic Agents
- Membrane Transport Modulators
- Acetylcholine Release Inhibitors
- Neuromuscular Agents
- Botulinum Toxins
- Botulinum Toxins, Type A
- abobotulinumtoxinA
Other Study ID Numbers
- 02-5458-A 04
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Chronic Male Pelvic Pain Syndrome
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Region StockholmKarolinska InstitutetRecruitingChronic Prostatitis With Chronic Pelvic Pain Syndrome | Chronic Prostatitis | Chronic Pelvic Pain Syndrome | Pelvic Floor; RelaxationSweden
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AJU Pharm Co., Ltd.OM Pharma SARecruitingChronic Prostatitis With Chronic Pelvic Pain Syndrome | Chronic Prostatitis | Chronic Pelvic Pain SyndromeKorea, Republic of
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State University of New York at BuffaloUniversity of California, Los Angeles; University of MichiganRecruitingChronic Pain | Interstitial Cystitis | Chronic Prostatitis | Bladder Pain Syndrome | Chronic Pelvic Pain Syndrome | Urologic Chronic Pelvic Pain Syndrome (UCPPS) | Chronic Overlapping Pain DisordersUnited States
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Al-Kindy College of MedicineCompletedChronic Prostatitis | Chronic Pelvic Pain SyndromeIraq
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Hisar Intercontinental HospitalCompletedChronic Prostatitis With Chronic Pelvic Pain SyndromeTurkey
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RAPbarcelonaCompletedChronic Pain | Pelvic Pain | Physical Therapy | Chronic Pain Syndrome | Pelvic Pain Syndrome | Chronic Pelvic Inflammatory DiseaseSpain
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University of WashingtonPaul G. Allen Family FoundationSuspendedProstatitis | Chronic Male Pelvic Pain SyndromeUnited States
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Weill Medical College of Cornell UniversitySociety of Interventional Radiology Foundation; EvideraEnrolling by invitationChronic Pelvic Pain Syndrome | Pelvic Congestive SyndromeUnited States
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Istanbul UniversityCompletedChronic Pelvic Pain SyndromeTurkey
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Xintian PharmaceuticalCompletedErectile Dysfunction | Chronic Prostatitis With Chronic Pelvic Pain SyndromeChina
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