Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07205445

Tensi+ European Registry

Status
Recruiting
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Stimuli Technology · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Tensi+ (Stimuli Technology, Boulogne Billancourt, France) is a newly released, medical transcutaneous-posterior tibial nerve stimulation (TC-pTNS) device marketed for overactive bladder (OAB) management. Preliminary studies have shown a favorable safety and efficacy profile. The goal of the present registry is to collect data among an important number of patients to assess the efficacy, safety and potential predictive factors of success in a current clinical setting over a total period of 1 year.

Conditions

Interventions

TypeNameDescription
DEVICETensi+Tensi+ (Stimuli Technology, Boulogne Billancourt, France) is a newly released, medical transcutaneous-posterior tibial nerve stimulation (TC-pTNS) device marketed for overactive bladder (OAB) management.

Timeline

Start date
2025-02-27
Primary completion
2027-10-01
Completion
2027-10-01
First posted
2025-10-03
Last updated
2025-10-03

Locations

17 sites across 3 countries: France, Italy, United Kingdom

Source: ClinicalTrials.gov record NCT07205445. Inclusion in this directory is not an endorsement.