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NCT03643380

Acute Study to Evaluate a Novel Implantable Midfield Powered Device in Humans With Urinary Incontinence

Completed Phase 1 Last updated 22 August 2018
What this trial tests

Phase 1 trial testing AHLeveeS System in Overactive Bladder in 6 participants. Completed in 30 January 2018.

Timeline
17 August 2017
Primary endpoint
15 November 2017
30 January 2018

Quick facts

Lead sponsorNeuspera Medical, Inc.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposedevice feasibility
Enrollment6
Start date17 August 2017
Primary completion15 November 2017
Estimated completion30 January 2018
Sites1 location across Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Neuspera Medical, Inc. — full company profile →

Who can join

Adults 18 to 65, any sex, with Overactive Bladder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A pre-market, prospective, non-randomized acute feasibility study for the treatment of patients with urinary incontinence (UI) as a consequence of urinary incontinence.

Publications & conference data

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

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Other recruiting trials for Overactive Bladder

Currently open trials in the same condition.

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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/NCT03643380.

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