Genetic Studies in Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS)

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Interstitial cystitis (IC), also called Bladder Pain syndrome (BPS) is a common condition with no known cause or cure. Twin studies and family accounts have suggested that the condition may be genetic or passed down (inherited) from one generation to another. In this study, the investigators are collecting genetic material via blood or saliva and medical information from families in North America in an attempt to identify genetic factors that may cause IC/BPS. The investigators are enrolling inviduals with IC/BPS and their family members (family members with and without IC like symptoms). Travel to Boston not required.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Healthy Volunteers: f
View:

• Diagnosis of IC/BPS

• Males and females of any age

• Urinary frequency - more than 1X/hour, and/or

• Dysuria, and/or

• Pelvic, suprapubic, or abdominal pain - for 3 months or longer

• Nocturia

• Normal urinary stream (by history)

• No evidence of active bacterial UTI (no pyuria \& negative urinary culture for last 3 months)

• First degree relative of someone with above symptoms

Locations
United States
Massachusetts
Boston Children's Hospital (BCH)
RECRUITING
Boston
Contact Information
Primary
Elicia A Estrella, MS, LCGC
elicia.estrella@childrens.harvard.edu
617-919-4552
Backup
Stephanie Brewster, MS, LCGC
Stephanie.Brewster@childrens.harvard.edu
Time Frame
Start Date: 2006-01-15
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 1000
Treatments
1 cohort
All participants will undergo genome sequencing and urinalysis studies.
Authors
Louis M Kunkel
Related Therapeutic Areas
Sponsors
Leads: Boston Children's Hospital

This content was sourced from clinicaltrials.gov

Similar Clinical Trials