Trial of Viagra' in Men With Chronic Pelvic Pain Syndrome Type III

Viagra is a potent 5-PDE inhibitor that causes vasodilation in the penis and, therefore, erection in men with erectile dysfunction. Our hypothesis is that Viagra may improve the symptoms of men with Chronic Pelvic Pain Syndrome based on the following assumptions:

Chronic Pelvic Pelvic Syndrome and Interstitial Cystitis involve poorly understood central and peripheral pain sensitization such as are seen in Chronic Sympathetic Dystrophy, also called Chronic Regional Pain Syndrome. This pain may be caused by constricted blood vessels resulting from past stress, injury or trauma

Viagra will dilate sympathetically constricted vessels and improve pelvic blood flow in the same manner it does in men with erectile dysfunction.

Since men with Chronic Pelvic Pain Syndrome often complain of sexual dysfunction; improving sexual function and, therefore, quality of life may improve overall well being and perception of pain.

Study Overview

• Status: Terminated
• Conditions: Prostatitis
• Intervention / Treatment: Drug: Viagra (sildenafil citrate)

Detailed Description

Screening Visit (Visit 1):

Patient will review and sign the study consent form. They will then be asked to complete study questionnaires regarding demographics, medical history, pelvic pain and psychological issues.

Urine will be collected and cultured for bacteria, gonorrhea and chlamydia . It will also be analyzed for white blood cells, NO and chemistry.

There will be a physical exam and prostate massage. During the prostate massage, expressed prostatic secretions will be collected and sent to the Male Fertility Lab for analysis.

Finally, he will be asked to go to the Male Fertility Lab to provide a semen sample.

Randomization:

After the subject's urine culture results have been reviewed (patient must be free of urinary tract infection to be in study), the Investigational Pharmacy will be asked to randomize the patient.

Pharmacy will then mail the patient's first month's study medication to him. He will also be mailed medication/voiding and pain diaries to fill out over the next month.

1. Month Visit (Visit 2):

   The subject will return to the Urology Clinic about 1 month after his Screening Visit (Visit 1). He will first fill out follow-up forms.

   Next, his previous month's empty medication container and completed diaries will be collected. A pill count will then be done

   Finally, the subject will receive his second month's study medication and medication/voiding and pain diaries.

2. Month Visit (Visit 3):

   Same as 1 Month Visit.

3. Month Visit (Visit 4):

First, the subject will be asked to fill out follow-up questionnaires

Next, the patient's caregiver will perform a physical exam and prostate massage during which, expressed prostatic secretions will be collected.

Then, his previous month's empty medication container and completed diaries will be collected. A pill count will then be done.

Finally, the subject will be sent to the Male Fertility Lab to collect a semen sample (as in Screening Visit).

12 Month Visit (Visit 5): With the exception of pill count, etc., same as Visit 3.

Dose:

• Active drug: Viagra, 50mg, orally, once a day, for 90 days
• Placebo: identically-appearing pill supplied by Pfizer

Concurrent Therapy:

_ No concurrent therapy will be offered

• Study Type: Interventional
• Enrollment: 30
• Phase: Phase 4

Contacts and Locations

Study Locations

• United States
  • Washington
    • Seattle, Washington, United States, 09195
      • University of Washington, Urology Clinic

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Male

Description

Inclusion Criteria:

• Diagnosis of male Chronic Pelvic Pain Syndrome Type III
• Age 18 - 65
• Pelvic pain duration of at least 3 months

Exclusion Criteria:

• Urinary tract infection within the last year
• Sexually transmitted disease within 3 months
• Antiviral therapy or antibiotics within the last 3 months
• Currently taking any medications or recreational drugs containing nitrates 3A4 inhibitors such as erythromycin, ketoconazole, or itraconazole
• Alpha-blocker therapy for treatment of high blood pressure or prostate problems
• Suffered a heart attack, stroke or life-threatening arrhythmia within the last months
• Cardiac failure or coronary artery disease causing unstable angina
• Resting hypotension (BP<90/50) or hypertension (BP>170/110)
• Patients with retinitis pigmentosa
• Kidney, liver or blood problems (including sickle cell anemia or leukemia)
• Allergy to sildenafil
• Deformed penis, Peyronie's disease or ever having had an erection lasting more than 4 hours
• Stomach ulcers or any types of bleeding problems
• Use of any other medical treatments that cause erections: pills, medicines that are injected or inserted into the penis, implants or vacuum pumps
• Back pain, unilateral testicular pain or rectal pain only
• Post-surgical pain
• Prostate biopsy or cystoscopy within 3 months
• Pain from another source in the genital tract, such as kidney stones or neoplasm
• History of prostate, bladder, renal or other urinary malignancies
• History of intravesical Bacillus Calmette-Guerin (BCG)
• Ulcerative colitis or Crohn's disease
• Radiation therapy to pelvis
• History of genitourinary tuberculosis
• Any neurological abnormalities including spinal cord injury and stroke
• Overtly psychotic or suicidal
• Unable to understand the protocol

In addition, subjects will be asked to refrain from having any new treatment for prostatitis during the study period, but will be allowed to remain on stable chronic therapy that they have been receiving for 3 or more months

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
NIH-CPSI -pain scores at 3 and 12 month post tx follow-up
AUA Score - at 3 and 12 month post tx follow-up

Secondary Outcome Measures

Outcome Measure
Graded Chronic Pain Scale (GCPS)-3 & 12 mo post tx f/u

Collaborators and Investigators

• Sponsor: University of Washington
• Collaborators: Berger, Richard E., M.D.
• Investigators: Principal Investigator: Richard E Berger, MD, Professor of Urology

Study record dates

Study Major Dates

• Study Start: July 1, 2004
• Study Completion: July 1, 2007

Study Registration Dates

• First Submitted: September 13, 2005
• First Submitted That Met QC Criteria: September 13, 2005
• First Posted (Estimate): September 19, 2005

Study Record Updates

• Last Update Posted (Estimate): October 22, 2008
• Last Update Submitted That Met QC Criteria: October 21, 2008
• Last Verified: October 1, 2008

More Information

Terms related to this study

• Keywords: Prostatitis
• Additional Relevant MeSH Terms: Pain; Neurologic Manifestations; Prostatic Diseases; Pelvic Pain; Prostatitis; Molecular Mechanisms of Pharmacological Action; Vasodilator Agents; Urological Agents; Enzyme Inhibitors; Phosphodiesterase Inhibitors; Phosphodiesterase 5 Inhibitors; Sildenafil Citrate
• Other Study ID Numbers: 03-9558-D 02