Adipose-derived SVF for Treatment of Alopecia
Completed · Not applicable
Conditions studied: Androgenetic Alopecia
In brief
The general objective of this study is to conduct a safety and feasibility study of a single injection of autologous adipose-derived SVF for the treatment of alopecia.
Key facts
- Study ID
- NCT02626780
- Run by
- GID BIO, Inc.
- People needed
- 7
- Starts
- 2016-07-20
- Expected to finish
- 2017-01-22
- Last updated by the study team
- 2019-03-21
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Males and females 18 - 60 years of age and older that have been diagnosed with androgenetic alopecia.
- Subjects will be in good health (ASA Class I-II) with a BMI < 35. Must have at least a 2cm x 2cm spot on the scalp which shows evidence of alopecia without scarring or traumatic injury
- Able and willing to make the required study visits.
- Able and willing to give consent and follow study instructions.
- Must speak, read and understand English
You may not qualify if…
- History of bleeding disorders, anticoagulation therapy that cannot be stopped 14 days prior to injection
- Allergic to lidocaine, epinephrine, valium or sodium phosphate
- Individuals with a propensity for keloids
- Individuals with diminished decision-making capacity will not be included in this research study
- Current use of anti-inflammatory or anticoagulation medications that affect bleeding or are for bleeding disorders. These include: Plavix, Warfarin (Coumadin, Jantoven, Marfarin). In addition, if any of the following medicines are used two (2) weeks prior to surgery the patient will be ineligible.
- Use of concomitant treatments, including topical medications, oral medications, meso-therapy, non-ablative fractional laser treatment, low-level laser therapy, interfollicular PRP injection and hair transplantation within the preceding 6 months.
- All smokers and other tobacco users.
Where it is running
- Maxwell Aesthetics — Nashville, Tennessee, United States
- Renew Associates — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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