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Topical 2-Deoxy-D-ribose Hydrogel Versus Minoxidil 5% Solution for Androgenetic Alopecia

Androgenetic alopecia is a common form of hair loss that can affect quality of life. This randomized controlled trial aims to evaluate the efficacy and safety of topical 2-Deoxy-D-ribose (2dDR) hydrogel compared with topical minoxidil 5% solution in the treatment of mild to moderate androgenetic alopecia in adults aged

Condition(s)Androgenic Alopecia
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryAndrogenetic alopecia is a common form of hair loss that can affect quality of life. This randomized controlled trial aims to evaluate the efficacy and safety of topical 2-Deoxy-D-ribose (2dDR) hydrogel compared with topical minoxidil 5% solution in the treatment of mild to moderate androgenetic alopecia in adults aged 18 to 50 years. Sixty participants will be randomized into 2 treatment groups. The 2dDR group will apply 1 gram of topical 2dDR hydrogel once daily to the affected scalp areas for 6 months. The minoxidil group will apply topical minoxidil 5% solution to the affected scalp areas for 6 months according to sex-specific dosing in the protocol. Participants will undergo clinical assessment, trichoscopic evaluation, and standardized scalp photography at baseline, Week 12, and Week
Who can participateInclusion Criteria: * Adults aged 18 to 50 years. * Male and female patients with androgenetic alopecia. * Mild to moderate disease severity, defined as Hamilton-Norwood scale II to V in males and Ludwig scale I to II in females. * Ability and willingness to provide written informed consent. Exclusion Criteria: * Other types of hair loss, including inflammatory or scarring alopecia. * Psoriasis. * Inflammatory scalp dermatoses. * History of severe systemic disease, including renal, cardiovascular, or hepatic disease. * Chemotherapy during the last 5 years. * Pregnancy. * Lactation. * Bleeding disorders.
Ages18 Years to 50 Years
SexAll
Lead sponsorKasr El Aini Hospital
LocationsCairo, Cairo Governorate, Egypt
Start date2026-01-01
NCT IDNCT07502976
Official listinghttps://clinicaltrials.gov/study/NCT07502976

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