Trials / Withdrawn
WithdrawnNCT05371951
Effect of Erchonia Laser on Erectile Dysfunction
A Pilot Evaluation of the Effect of the Erchonia® HLS™ on Individuals With Erectile Dysfunction
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Erchonia Corporation · Industry
- Sex
- Male
- Age
- 40 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This study is to see if applying low-level laser light can provide improvement in erectile dysfunction
Detailed description
The purpose of this pilot study is to determine the effectiveness of the Erchonia® HLS™, manufactured by Erchonia Corporation (the Company), in providing improvement in erectile dysfunction.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Erchonia HLS | 84 procedure administrations with the Erchonia® HLS™ administered by the subject at home: twice daily procedure administrations for 6 weeks. |
Timeline
- Start date
- 2021-10-05
- Primary completion
- 2023-03-01
- Completion
- 2023-03-01
- First posted
- 2022-05-12
- Last updated
- 2023-03-23
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05371951. Inclusion in this directory is not an endorsement.