Last reviewed · How we verify
NCT05647694
V-NAV Usability Study: End Users Trying the Vortant Indoor Navigation Tool
NA trial testing V-NAV indoor navigation prototype in Blindness and Low Vision in 16 participants. Suspended.
30 April 2025
Quick facts
| Lead sponsor | Vortant Technologies, LLC |
|---|---|
| Phase | NA |
| Status | Suspended |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | other |
| Enrollment | 16 |
| Start date | 1 January 2025 |
| Primary completion | 30 April 2025 |
| Estimated completion | 30 April 2025 |
| Sites | 1 location across United States |
Drugs / interventions tested
- V-NAV indoor navigation prototype
Conditions studied
- Blindness and Low Vision — all drugs for Blindness and Low Vision →
Sponsor
Vortant Technologies, LLC
Who can join
12 and older, any sex, with Blindness and Low Vision. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The study will begin with an explanatory/training session where individuals with low vision will learn to use the V-NAV (Vortant NAVigation tool) indoor navigation app, and will have the opportunity to try it for a few representative tasks. The main activity includes a take-home trial, an extended unstructured period to emulate the post-purchase experience of users, during which participants will have the opportunity to use the V-NAV in their everyday lives. Data will be collected from the users to measure the relative advantage of V-NAV compared to the user's current indoor navigation method.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05647694
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Blindness and Low Vision
Currently open trials in the same condition.
- NCT06477809 — A Pilot Study Comparing Performance of Blind Participants on 12 Tasks, With and Without the ARIA Device · NA · recruiting
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 NCT05647694 (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 Vortant Technologies, LLC
- Last refreshed: 25 November 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/NCT05647694.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing