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Clinical Trial Summary

Evaluation of Safety and efficacy of autologous stromal vascular fraction derived from denovo versus platelet rich plasma enhanced donner site in treatment of male androgenic alopecia


Clinical Trial Description

40 Patients with androgenic alopecia will be randomly divided into 2 groups Group A (20): will receive 2 session of stromal vascular fraction directly after fat harvesting and processing and stromal vascular fraction extraction with 1 month interval . Group B(20): will be injected with 2 session of Platelet rich plasma 3weeks interval at site of fat harvesting and will be followed 1 month later with fat aspiration from site where Platelet rich plasma was previously injected and this fat will undergo fat processing and stromal vascular fraction extraction followed by 2 session of stromal vascular fraction injection at scalp 1month interval . Patients at both groups will receive topical and systemic antibiotics after stromal vascular fraction injection . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06326359
Study type Interventional
Source Sohag University
Contact dina A mahmoud, assistant lecturer
Phone 01097185631
Email dr.dondon123@gmail.com
Status Not yet recruiting
Phase N/A
Start date March 2024
Completion date October 2026

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