None listed
Conditions
Brief summary
OBJECTIVE This study aims to compare the efficacy of exosomes versus PRP in the treatment of Androgenetic alopecia by using photographic assessment, hair pull test and patient self-assessment questionnaire over a period of 6 months. HYPOTHESIS Exosomes are expected to be significantly more effective then PRP in treatment of AGA.
Interventions
This study aims to compare the efficacy of exosomes versus PRP in the treatment of Androgenetic alopecia by using photographic assessment, hair pull test and patient self-assessment questionnaire over a period of 6 months. The enrolled patients will be randomly divided into two groups using the lottery method, Group A and B, each with 40 participants. GROUP A: Group A will receive treatment with exosomes intradermally at 0,1 and 3 months. Exosomes used are GFC CELL, consist of Leucoexo 97% having GFC CELL EXO SCALP 9700 powder and EXO SCALP Pep9 solution. The scalp will be cleaned with spirit and nerve block will be given by using the local injection, lignocaine, by insulin syringe at supratrochlear, supraorbital, and occipital region. Exosomes will then be injected at a strength of 2 to 10 billion particles/5ml, at a dose of 0.1 ml/cm2 of scalp. Patients will be observed for 1-hour post procedure for any adverse effects and will be instructed not to wash or massage their hair and avoid heavy activities for 48 hours after the injection. Exosomes will be administered by Dermatologist in the dermatology clinic, Combined Military Hospital, Quetta. Participants will be assessed at 0,1, 3, and 6 months. Serial photographs will be taken at each assessment. The efficacy of both groups will be evaluated using the hair pull test, global photography, patient and physician satisfaction questionnaire.
Sponsors
Study design
Eligibility
Inclusion criteria
Inclusion criteria Clinical diagnosis of AGA Age range of 18-60 years Platelets count more than 150, 000 /µl to 450,000/ µl Patients with Hamilton-Norwood Grade 2-5 or Ludwig scale Grade 1-3 Patients who haven’t received topical or systemic treatments for AGA within 3 months prior to the study Patient who gave consent for the study
Exclusion criteria
Exclusion criteria Patients with other causes of hair loss fungal infection such as fungal infection, inflammatory or scarring alopecia, hyper-androgenism, telogen effluvium or other hormonal disorders Patients with history of severe systemic disease (renal, cardiovascular hepatic and lungs) or active cancers Pregnant or breastfeeding patients Patients having known hypersensitivity to exosomes Patients that are immunodeficient or are undergoing immunosuppressive therapy Patients on anticoagulation or having bleeding disorders such as thrombocytopenia and anemia