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Clinical Trials/ISRCTN22433402
ISRCTN22433402CompletedPhase 4

Efficacy and safety of fesoterodine fumarate in neurogenic detrusor overactivity due to spinal cord lesion (SCL) or multiple sclerosis (MS)

ational Rehabilitation Center0 sites85 target enrollmentStarted: June 2, 2016Last updated:
Conditions

Trial Snapshot

Phase
Phase 4
Status
Completed
Sponsor
Enrollment
85

Study Overview

Brief Summary

2021 Results article in https://doi.org/10.1002/nau.24790 (added 02/03/2022)

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
All

Inclusion Criteria

  • 1. Aged between 18-80 years old
  • 2. Suffering from neurogenic detrusor overactivity, confirmed by urodynamics testing, secondary to MS or SCI of at least 6 months prior to enrollment
  • 3. Patients suffering from MS should be clinically stable for at least 3 months prior to enrollment

Exclusion Criteria

  • 2. History of urothelial cancer
  • 3. Urolithiasis
  • 4. Stress incontinence
  • 5. Interstitial cystitis
  • 6. Pelvic organ prolapsed (= III grade)
  • 7. Prior pelvic surgery or pelvic radiation treatment
  • 8. Uncontrolled narrow angle glaucoma
  • 9. Pregnancy
  • 10. Dementia

Investigators

Sponsor
ational Rehabilitation Center

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