Planta Med 2008; 74(12): 1430-1435
DOI: 10.1055/s-2008-1081338
Clinical Studies
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Double-Blind Clinical Trial for Evaluating the Effectiveness and Tolerability of Ageratina pichinchensis Extract on Patients with Mild to Moderate Onychomycosis. A Comparative Study with Ciclopirox

Ofelia Romero-Cerecero1 , 2 , Alejandro Zamilpa1 , Jesús Enrique Jiménez-Ferrer1 , Gabriela Rojas-Bribiesca1 , Rubén Román-Ramos2 , Jaime Tortoriello1
  • 1Centro de Investigación Biomédica del Sur, Instituto Mexicano del Seguro Social (IMSS), Morelos, México
  • 2Programa de Doctorado en Ciencias Biológicas, División de Ciencias Biológicas y de la Salud. Universidad Autónoma Metropolitana, México, D.F.
Further Information

Publication History

Received: April 23, 2008 Revised: June 26, 2008

Accepted: June 29, 2008

Publication Date:
31 July 2008 (online)

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Abstract

Aerial parts of Ageratina pichinchensis have been used, in Mexican traditional medicine, as a remedy for the treatment of skin mycosis. Onychomycosis, also known as tinea of the nails or tinea unguium, constitutes an infection of the nails produced by dermatophytes. Clinically, onychomycosis is manifested by changes on the color, texture and thickness of the nail. The agent most frequently found in this disease is Tricophyton rubrum. The present study evaluated the therapeutic effectiveness and tolerability of topical administration of A. pichinchensis extract on the nails of patients with the clinical and mycological diagnosis of onychomycosis. A phytopharmaceutical formulation was developed in a lacquer solution containing the standardized (encecalin) extract of A. pichinchensis. A similar lacquer solution containing 8 % ciclopirox was used as control. Treatments were assigned randomly and administered topically for 6 months. Ninety six patients concluded the study (49 in the experimental group and 47 in the control); 71.1 % of patients from the experimental and 80.9 % from the control group showed therapeutic effectiveness, while 59.1 % and 63.8 % from the experimental and control group, respectively, achieved mycological effectiveness. Therapeutic success was observed in 55.1 and 63.8 %, respectively. No patient exhibited intense side effects. Statistical analysis demonstrated no differences between treatments.

References

Dr. Ofelia Romero Cerecero

Centro de Investigación Biomédica del Sur

Instituto Mexicano del Seguro Social (IMSS)

Argentina No. 1

62790 Xochitepec

Morelos

México

Phone: /Fax: +52-777-361-2155

Email: orcerecero@yahoo.com.mx