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NCT01920178 · ClinicalTrials.gov registry record · NA
Evaluation Study for the Efficacy and Safety of PinPointe FootLaser in Treatment for Onychomycosis
A NA study, sponsored by Cambridge Health Alliance.
- Terminated
- Registry status
- NA
- Development phase
- 7
- Enrollment target
NCT01920178: Clinical Trial NA study, sponsored by Cambridge Health Alliance.
NCT01920178 is a NA study that was terminated before completion, run by Cambridge Health Alliance. The registered enrollment target is 7 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01920178, a NA study, was terminated before completion, sponsored by Cambridge Health Alliance.
- TERMINATED
- Registry status
- NA
- Development phase
- 7 participants
- Enrollment target
Study Summary
The purpose of this study is to assess the clinical efficacy and safety of the PinPointe Foot Laser device for the treatment of patients with onychomycosis who have been previously treated with oral Terbinafine and failed.
Interventions
- DEVICE PinPointe Foot Laser
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 7 participants |
| Start Date | 2013-04 |
| Est. Completion | 2015-05 |
| Phase | NA |
Why NCT01920178 stopped before completion
NCT01920178 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 1 intervention - of which PinPointe Foot Laser is the first listed.
NCT01920178 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01920178 about?
NCT01920178 is a clinical study titled "Evaluation Study for the Efficacy and Safety of PinPointe FootLaser in Treatment for Onychomycosis". The purpose of this study is to assess the clinical efficacy and safety of the PinPointe Foot Laser device for the treatment of patients with onychomycosis who have been previously treated with oral Terbinafine and failed.
What is the current status of trial NCT01920178?
This trial is currently terminated. It is a NA study. The enrollment target is 7 participants. The study started on 2013-04. Estimated completion is 2015-05.
What interventions are being tested in trial NCT01920178?
The interventions under investigation include: PinPointe Foot Laser (DEVICE).
Who is sponsoring clinical trial NCT01920178?
This trial is sponsored by Cambridge Health Alliance, which has 45 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01920178's enrollment target sits among peer trials
7 1982nd of 2000 higher than 18 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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