Evaluating the Topical Herbal Solution on the Treatment of Male Pattern Hair Loss and Comparison With Minoxidil 5%

• Status: Completed
• Trial end date: 2019-09-02
• Target enrollment: 0
• Participant gender: Male

Summary

The purpose of this study is evaluating the efficacy and safety of a topical herbal solution in males for the treatment of Androgenetic alopecia.

• Phase: Phase 3
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Farid Masoud
• Treatments: Minoxidil; Pharmaceutical Solutions

Criteria

Inclusion Criteria:

• Men 18 to 50 years old

• Written consent

• Normal general health status

• Men who have a presentation of androgenetic alopecia (Norwood II - V).

Exclusion Criteria:

• Use of any topical product in the target region interfering with the study product in the last three months

• Within the past 6 months receiving of chemotherapy/cytotoxic agents

• Clinical diagnosis of alopecia areata or other non-AGA forms of alopecia

• Uncontrolled hypertension

• Any dermatological disorders in the scalp, such as fungal or bacterial infections, eczema, atopic dermatitis, seborrheic dermatitis, psoriasis, sun damage, skin cancer

• Hormonal diseases such as thyroid disorders, diabetes and, ...

• Smokers

• Liver and kidney disease

• History of hair transplants

• History of surgical correction of hair loss on the scalp

• Subject having dyed, bleached hair or, with a permanent wave prior to study start.

• No written consent