A Clinical Study to Evaluate the Efficacy and Safety of Ultra in Promoting Hair Regrowth
Part of paid clinical trials in Glenview, Illinois.
- Sponsor
- CynosureLutronic
- Study ID
- NCT07588243
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 22 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Low Level Laser Therapy — DEVICEStudy participants received a total of 6 low level laser therapy treatments on their scalp. The treatments occurred 2 weeks apart (+/- 3 days).
Study Details
The goal of this clinical study is to evaluate the efficacy and safety of the Ultra device for the treatment of hair regrowth by assessing the improvement of hair density and hair shaft diameter.
Key Dates
- Start date
- Feb 19, 2026
- Status verified
- May 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 44 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Ultra Treatment
Primary Outcome Measure
Difference in the Change in Hair Density from Baseline vs 90-day Follow-up [ Time Frame: From baseline (treatment 1) to the 90 day follow up after treatment 6. ]
Central Contacts
- Charlotte Antoni Clinical Research Coordinator9786276614
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Dy Dermatology | Glenview | Illinois | 60025 | |
| Cynosure Lutronic | Westford | Massachusetts | 01886 |
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