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 — DEVICE
    Study 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

Locations (2)

FacilityCityStateZIPSite coordinators
Dy DermatologyGlenviewIllinois60025
Lady Christine Dy, MD
847-832-1185
Cynosure LutronicWestfordMassachusetts01886
Omar A. Ibrahimi, M.D., Ph.D.
203-428-4440

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