Chemokine Mechanisms in Chronic Pelvic Pain

Completed

Conditions studied: Chronic Prostatitis With Chronic Pelvic Pain Syndrome, Prostatitis

In brief

The purpose of this study is to identify biomarkers that can be utilized in the diagnosis of chronic pelvic pain syndrome in men.

Key facts

Study ID

NCT01676857

Run by

Northwestern University

People needed

147

Starts

2010-05-01

Expected to finish

2019-01-24

Last updated by the study team

2019-03-13

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: accepted.

You may qualify if…

• CP/CPPS group inclusion criteria
• Patients are eligible for the study if they meet the following criteria:
• Participant has signed and dated the appropriate Informed Consent document.
• Agreed to participate in Study procedures.
• Participant is at least 18 years of age.
• Participant reports a response of at least 1 on the pain, pressure or discomfort scale (SYM-Q, Question #1).
• Participant reports pain or discomfort in any of the 8 domains of the Male Genitourinary Pain Index (MGUPI) (items 1a, 1b, 1c, 1d, 2a, 2b, 2c, 2d).
• These CP/CPPS symptoms been present for the majority of the time during any 3 months in the previous 6 months.

You may not qualify if…

• Participant has an on-going symptomatic urethral stricture.
• Participant has an on-going neurological disease or disorder affecting the bladder or bowel fistula.
• Participant has a history of cystitis caused by tuberculosis, radiation therapy or Cytoxan/cyclophosphamide therapy.
• Participant has augmentation cystoplasty or cystectomy.
• Participant has a history of cancer (with the exception of skin cancer).
• Participant has current major psychiatric disorder or other psychiatric or medical issues that would interfere with study participation (e.g. dementia, psychosis, upcoming major surgery, etc).
• Participant diagnosed with unilateral orchialgia, without pelvic symptoms.
• Participant has a history of transurethral microwave thermotherapy (TUMT), transurethral needle ablation (TUNA), balloon dilation, prostate cryo-surgery, or laser procedure.
• Control group exclusion criteria In addition to the exclusion criteria listed above additional criteria for control subjects are as follows.
• In the past year, symptoms of discomfort or pain in the pelvic region for extended periods of time.
• Volunteers who have had a urinary tract infection with a urine culture value of >100,000 CFU/ml within the past three months.
• Volunteers treated with intravesical chemotherapy or BCG.
• Volunteers who have had any of the following sexually transmitted diseases (STDs) - gonorrhea, chlamydia, mycoplasma or trichomonas.
• Volunteers with inflammatory bowel disease (such as Crohn's disease or ulcerative colitis, but not irritable bowel syndrome)

Where it is running

• Northwestern Medical Faculty Foundation — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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