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NCT06085846
Real-World Registry - The Vivally® System
trial testing Vivally® System Wearable, Non-Invasive Neuromodulation System, and Mobile Application in Urinary Incontinence in 5,000 participants. Enrolling by invitation.
1 July 2043
Quick facts
| Lead sponsor | Avation Medical, Inc. |
|---|---|
| Status | ENROLLING BY INVITATION |
| Study type | OBSERVATIONAL |
| Enrollment | 5,000 |
| Start date | 14 July 2023 |
| Primary completion | 1 July 2043 |
| Estimated completion | 1 July 2043 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Vivally® System Wearable, Non-Invasive Neuromodulation System, and Mobile Application
Conditions studied
- Urinary Incontinence — all drugs for Urinary Incontinence →
- Urinary Urge Incontinence — all drugs for Urinary Urge Incontinence →
Sponsor
Avation Medical, Inc.
Who can join
18 and older, any sex, with Urinary Incontinence or Urinary Urge Incontinence. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a Real-World Registry Study to collect real-world dosing, utilization, demographic, quality of life, and data from the e-bladder diaries of patients utilizing the Vivally® System. Data points will be drawn from the Avation Medical HIPAA-compliant cloud database including but not limited to: Therapy compliance and stimulation metrics Diary entries provided by patients Various questionnaires Participants have the option to opt out of allowing their data to be part of any publication at any time.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06085846
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Urinary Incontinence
Currently open trials in the same condition.
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- NCT07426861 — Pre-Operative Nurse-Led Education With Direct Physiotherapy Referral to Reduce Post-Prostatectomy Incontinence · NA · recruiting
- NCT07413692 — BTL-699-2 and HPM-6000UF Devices for the Improvement of Depressive Symptoms and Urinary Incontinence in Postpartum and E · NA · recruiting
- NCT07413705 — BTL-699-2 and HPM-6000UF Devices for the Improvement of Depressive Symptoms and Sexual Function Among Perimenopausal and · NA · recruiting
Other Avation Medical, Inc. trials
Trials by the same sponsor.
- NCT05381116 — A Sham-Controlled Study to Evaluate the Safety and Efficacy of a Smart, Self-Adjusting, Surgery-Free, Wearable Bladder N · NA · terminated
- NCT04547920 — FREEOAB Study for Overactive Bladder · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06085846 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Avation Medical, Inc.
- Last refreshed: 29 May 2024
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/NCT06085846.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing