At a glance
ClinicalIndex Comparison RecordN/ACompleted· 44 enrolled
Drug / intervention
Handi-Dome Laser +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Novel Approach to Treating Androgenetic Alopecia in Females With Low Level Laser Therapy
In Brief
A clinical study evaluating Handi-Dome Laser and Incandescent red light source. for Androgenetic Alopecia. Completed, enrolled 44 participants across 2 sites.
Detailed Summary
This study will acquire data on hair growth of the head that is the result of treatment with a non-heat generating, laser product. This data will come from counting of terminal hairs before treatment begins and after treatment is completed. The treatment regime is every other day for 16 weeks.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAndrogenetic Alopecia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedOct 2013
Enrollment StartMar 2014
Primary CompletionAug 2014
Study CompletionSep 2014
TodayJul 2026
First PostedOct 22, 2013
Enrollment StartMar 1, 2014
Primary CompletionAug 1, 2014
Study CompletionSep 1, 2014
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 12.7 years ago
Interventions
Handi-Dome Laserdevice
One, 30 minute treatment, every other day for 16 weeks.
Incandescent red light source.device
One, 30 minute treatment, every other day for 16 weeks.