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Clinical Trials/NCT03023241
NCT03023241
Completed
N/A

Diagnosis of Bladder Pain Syndrome / Interstitial Cystitis

Cantonal Hospital, Frauenfeld1 site in 1 country300 target enrollmentDecember 2004

Overview

Phase
N/A
Intervention
Not specified
Conditions
Bladder Pain Syndrome
Sponsor
Cantonal Hospital, Frauenfeld
Enrollment
300
Locations
1
Primary Endpoint
Identification of new diagnostic markers for BPS/IC
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

To identify new, simple and reliable biomarkers for bladder pain syndrome/interstitial cystitis (BPS/IC) for diagnosis of this disease.

Detailed Description

Collection and analyses of bladder biopsies, bladder washings, blood and urine samples of patients with bladder pain syndrome/interstitial cystitis (BPS/IC), overactive bladder syndrome (OAB) and bladder-healthy controls. Analyses include ELISA, RT-qPCR, DNA sequencing, and immunohistochemistry techniques. Differences between patient groups are statistically evaluated.

Registry
clinicaltrials.gov
Start Date
December 2004
End Date
July 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Cantonal Hospital, Frauenfeld
Responsible Party
Principal Investigator
Principal Investigator

Prof. Dr. Volker Viereck

Prof. Dr. med.

Cantonal Hospital, Frauenfeld

Eligibility Criteria

Inclusion Criteria

  • patient with diagnosed BPS/IC, OAB or healthy controls
  • included healthy controls must have another pelvic surgery planned (e.g. hysterectomy)
  • being able to act and judge

Exclusion Criteria

  • unstable endocrinological situation
  • severe illness

Outcomes

Primary Outcomes

Identification of new diagnostic markers for BPS/IC

Time Frame: 2 days

Secondary Outcomes

  • Identification of molecular details that lead to BPS/IC (pathogenesis).(2 days)

Study Sites (1)

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