Skip to content

Microbiome of Urologic Chronic Pelvic Pain Syndrome

WithdrawnNCT03027076
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This research is being done to learn more about the bacteria that live in the genito-urinary tract in subjects with urologic chronic pelvic pain syndrome (UCPPS).

Study details

Official title
Microbiome Studies of Urologic Chronic Pelvic Pain Syndrome
Interventions
  • Procedure: Genitourinary Specimen Collection
  • Procedure: Collect midstream urine samples
Sponsor
Johns Hopkins University
Start date
2013-11
Primary completion
2015-01
Sex
All
Age range
from 18 Years to 70 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Consent: Participant has signed and dated the Informed Consent document, approved by the Johns Hopkins Medical Institutions Institutional Review Board; * Agreement: Participant agrees to participate in study procedures; * Age: Participant is at least 18 years of age; * Symptom Severity: Participant reports a response of at least 8 on the Pain Domain of the NIH-Chronic Prostatitis Symptom Index (CPSI) Questionnaire; * Duration of Symptoms: Symptoms have been present for at least 3 months within the preceding 6 months. Exclusion Criteria: * Urethral conditions: Participant has an ongoing symptomatic urethral stricture; * Bladder conditions: Participant has a history of cystitis caused by tuberculosis, radiation therapy or cytoxan/cyclophosphamide therapy, augmentation cystoplasty or cystectomy; * Testicular conditions: Participant diagnosed with unilateral orchialgia, without pelvic symptoms; * Prostate conditions or procedures: Participant has a history of transurethral microwave thermotherapy (TUMT), transurethral needle ablation (TUNA), balloon dilation, prostate cryosurgery, or laser procedure; * Neurological diseases or disorders affecting the bladder: Parkinson disease, multiple system atrophy, multiple sclerosis, spinal cord injury, cervical myelopathy, acute transverse myelitis, diabetic cystopathy, or dysfunctional voiding (non-neurogenic neurogenic bladder or Hinman syndrome); * Psychiatric conditions: 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.); * Malignancy: Participant has a history of cancer (with the exception of skin cancer). Control group exclusion criteria: In addition to the exclusion criteria listed above, additional criteria for control subjects are as follows: * Chronic Pain: In the past year, symptoms of discomfort or pain in the pelvic region for a period longer than 3 months within the preceding year; * Infection: Volunteers who have had a urinary tract infection with a urine culture value of \>100,000 colony forming units/ml (CFU/ml) within the past three months. * Intravesical Therapy: Volunteers treated with intravesical chemotherapy or Bacillus Calmette-Guerin (BCG) therapy; * Gastrointestinal Conditions: Volunteers with inflammatory bowel disease (such as Crohn's disease or ulcerative colitis, but not irritable bowel syndrome).

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03027076