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S1P1 Receptor Subtype (S1PR1) Axis in Patients With Interstitial Cystitis (IC) Pain

NCT03003845 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 21

Last updated 2021-07-23

No results posted yet for this study

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.

Conditions

  • Interstitial Cystitis

Interventions

OTHER

Questionnaires

QOL and pain questionnaires will be given to patients at 3, 6, and 12 months post surgery

OTHER

Collection of Blood samples

Blood for PBLs will be collected at 3, 6, and 12 months post surgery

Sponsors & Collaborators

  • St. Louis University

    lead OTHER

Principal Investigators

  • Eugen C Campian, MD · St. Louis University

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-26
Primary Completion
2020-02-27
Completion
2020-02-27

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03003845 on ClinicalTrials.gov