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NCT05211193

Open Label Study to Evaluate the Efficacy of the Home Based Electrical Transcutaneous URIS I in the Treatment of Overactive Bladder (OAB).

Completed Last updated 17 February 2022
What this trial tests

trial testing eTNM delivered by URIS I nerve stimulation device in Overactive Bladder (OAB) in 40 participants. Completed in 2 November 2020.

Timeline
8 January 2020
Primary endpoint
28 April 2020
2 November 2020

Quick facts

Lead sponsorStimvia s.r.o.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment40
Start date8 January 2020
Primary completion28 April 2020
Estimated completion2 November 2020
Sites1 location across Czechia

Drugs / interventions tested

Conditions studied

Sponsor

Stimvia s.r.o.

Who can join

18 and older, female only, with Overactive Bladder (OAB) or Failed Any OAB Pharmacotherapy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Open label Study to Evaluate the Efficacy of the Home Based Electrical Transcutaneous NeuroModulation (eTNM) Treatment Via Nerve Stimulator URIS I in the Treatment of Overactive Bladder.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Overactive Bladder (OAB)

Currently open trials in the same condition.

Other Stimvia s.r.o. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05211193.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing