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Clinical Trial Summary

For each patient in the study, blood, and pain scores will be collected to look for markers for pain, at the start of treatment and 6 months after surgery of treatment.

Clinical Trial Description

The study is investigator-initiated, prospective, study. There will be no change in care. Patients who have had a diagnosis of IC made by cystoscopy and hydrodistension and still have pain will be recruited for this study. Patients will have blood samples taken at the visit they sign the consent form and 6 months later. The study staff will call and remind the patient of their 6 month visit. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT03003845
Study type Observational [Patient Registry]
Source St. Louis University
Status Completed
Start date February 26, 2019
Completion date February 27, 2020

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