Health Condition 1: L649- Androgenic alopecia, unspecified
Conditions
Interventions
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: All patients clinically diagnosed as androgenic alopecia Norwood Hamilton grades III â?? V or Ludwigs II- III (in case of female pattern hair loss) Age above 25 yrs with active hair loss in the past 6 months Should have adequate adipose tissue for syringe based lipoharvest Patients willing to undergo procedure after a written informed consent and complete blood check up with serology Who have not undergone any interventional procedures up till now over scalp
Exclusion criteria
Exclusion criteria: Not willing to undergo the procedures Any abnormality in coagulation profile and serology Diabetes, hypertension and any other significant comorbidities (clinically significant medical / psychiatric illness) With active infection/ inflammation/ auto immune focus
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement in Androgenetic alopecia and Female patterned hair loss assessed by trichoscopic parameters Baseline, 3 months and 6 months after the administration of Autologous SVF and post scalp threads in patients who have undergone SVFTimepoint: After 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the efficacy of SVF in androgenetic alopecia after 3 months To assess the superiority of combination of scalp threads and SVF over individual modalities.Timepoint: After 3 months After 6 months | — |
Countries
India
Contacts
CUTIS Academy of Cutaneous Sciences