Trans-MAPP Study of Urologic Chronic Pelvic Pain: Control Study Protocol
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Interstitial Cystitis
- Sponsor
- University of Pennsylvania
- Enrollment
- 72
- Locations
- 6
- Primary Endpoint
- Urinary Severity Score
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
The Multidisciplinary Approach to the Study of Chronic Pelvic Pain (MAPP) Research Network has been established by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the National Institutes of Health (NIH) to focus on a broader approach to the study of Interstitial Cystitis (IC)/ Bladder Pain Syndrome (BPS) in men and women, and Chronic Prostatitis (CP)/Chronic Pelvic Pain Syndrome (CPPS) in men, than previously undertaken. Patients with IC or CP are being recruited for a new study called the "Trans-MAPP Study of Urologic Chronic Pelvic Pain: Symptom Patterns Study (SPS). This research study will recruit Control Participants to better understand the symptoms of individuals with some form of IC or CP. As with many chronic pain disorders, IC and CP are poorly understood, and treatment is often not helpful. The goal of this study is to better understand how pain is felt in people with IC or CP and the investigators hope that this study will lead to improvement in the treatment of IC and CP.
Detailed Description
Urological Chronic Pelvic Pain Syndromes (UCPPS) are characterized by pelvic pain with concurrent urinary symptoms. Broadly, UCPPS comprise Interstitial Cystitis/Painful Bladder SyndromeBladder Pain Syndrome (IC/BPS) in men and women, and Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) in men. IC is a debilitating bladder disorder characterized by urinary urgency, frequency, and pain. The presentation of symptoms can be quite variable among patients, suggesting that IC is a multi-factorial syndrome with several proposed etiologies, some of which may be interrelated.1 BPS as defined by the International Continence Society, is "the complaint of suprapubic pain related to bladder filling, accompanied by other symptoms, such as increased daytime and night-time frequency, in the absence of proven urinary infection or other obvious pathology."2 BPS is a clinical description of disease based on the patient's symptoms, and does not depend on urodynamic or cystoscopic findings. These symptoms may be related to IC, although diagnostic criteria are still lacking for this entity, and the relationship between BPS and IC is not clear. After the initiation phase for the MAPP SPS Study, it became clear that many of the hypotheses being proposed required well-characterized healthy "normal" controls that lack urologic pain as well as other study related symptoms/conditions. This second phase is enriched with pre-defined subgroups and a longer follow-up period which will allow further investigation of clinical and biologic factors associated with worsening and/or improvement of reported urinary and non-urinary symptoms.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Participant has signed and dated the appropriate Informed Consent document.
- •Agreed to participate in ALL required study procedures (including Biospecimen collections, Neuroimaging, and Quantitative Sensory Testing).
- •Gave permission for use of DNA for genetics studies.
- •Gender recorded in Participant Registration module.
- •Participant is at least 18 years of age.
- •Participant is able to speak, read, and understand English.
- •Participant reports a response of "0" (zero) on the pain, pressure or discomfort scale (SYM-Q, Question #1).
- •Participant reports no chronic pain in the pelvic or bladder region, and reports no chronic pain in any other body region.
- •Participant reports no urological symptoms that have been evaluated, but are still present.
Exclusion Criteria
- •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 an active autoimmune or infectious disorder (such as Crohn's Disease or Ulcerative Colitis, Lupus, Rheumatoid Arthritis, Multiple Sclerosis, or HIV).
- •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 has severe cardiac, pulmonary, renal, or hepatic disease that in the judgment of the study physician would preclude participation in this study.
- •Participant has had definitive treatment for acute epididymitis, urethritis, vaginitis.
- •Participant has history of unevaluated hematuria, this will require the evaluation of a study physician to determine if this has been appropriately evaluated.
Outcomes
Primary Outcomes
Urinary Severity Score
Time Frame: 6 months
The outcome measures are the same scores which will be used to compare normal The scores for urinary severity in healthy individuals with scores of those with a diseased state (i.e. individuals with UCPPS
Pain Severity Score
Time Frame: 6 months
The outcome measures are the same scores which will be used to compare normal The scores for pain severity in healthy individuals with scores of those with a diseased state (i.e. individuals with UCPPS)