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Diagnosis of Bladder Pain Syndrome / Interstitial Cystitis

C

Cantonal Hospital, Frauenfeld

Status

Completed

Conditions

Interstitial Cystitis
Bladder Pain Syndrome
Overactive Bladder

Treatments

Procedure: biopsy

Study type

Interventional

Funder types

Other

Identifiers

NCT03023241
9900.013 BPS/IC study
KEKTGOV2010/01 (Other Identifier)

Details and patient eligibility

About

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

Full 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.

Enrollment

300 patients

Sex

Female

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

300 participants in 1 patient group

all study patients
Experimental group
Description:
Same intervention for all subjects: anamnesis, questionnaires and biological samples (bladder biopsy, bladder washing, blood and urine) are collected at one single visit.
Treatment:
Procedure: biopsy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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