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Clinical safety and tolerability evaluation of Withania somnifera (L.) Dunal (Ashwagandha) root extract in healthy human volunteers.
Vaidya, Vidyadhar G; Gothwad, Amol; Ganu, Gayatri; Girme, Aboli; Modi, Siddharth J; Hingorani, Lal.
Afiliación
  • Vaidya VG; Lokmanya Medical Research Centre and Hospital, Pune, 411033, Maharashtra, India.
  • Gothwad A; Lokmanya Medical Research Centre and Hospital, Pune, 411033, Maharashtra, India.
  • Ganu G; Mprex Healthcare Pvt. Ltd., Pune, 411057, Maharashtra, India.
  • Girme A; Pharmanza Herbal Pvt. Ltd., Anand, 388430, Gujarat, India.
  • Modi SJ; Pharmanza Herbal Pvt. Ltd., Anand, 388430, Gujarat, India.
  • Hingorani L; Pharmanza Herbal Pvt. Ltd., Anand, 388430, Gujarat, India. Electronic address: lal@pharmanzaherbals.com.
J Ayurveda Integr Med ; 15(1): 100859, 2024.
Article en En | MEDLINE | ID: mdl-38154316
ABSTRACT

BACKGROUND:

Withania somnifera (L.) Dunal, known as Ashwagandha, is an adaptogen with significant importance in Ayurveda for its potential health benefits in strength ('balavardhan') and muscle growth ('mamsavardhan'). Despite numerous studies on its efficacy, limited research is reported on its clinical safety and tolerability in healthy individuals.

OBJECTIVE:

This research evaluated the tolerability and safety of standardized Withania somnifera root extract (WSE) capsules (AgeVel®/Witholytin®) at 1000 mg/day dose upon oral administration in healthy male participants.

METHOD:

A non-randomized, open-label, single-treatment clinical study included eighteen healthy male participants aged 18 to 60. The participants were administered a dose of 500 mg of the WSE capsules twice daily for four weeks. Each capsule contained not less than 7.50 mg of total withanolides. The study evaluated various indicators in a cohort of healthy participants throughout the trial, including vital signs, organ function tests, urine analysis, X-ray and ECG, cardiorespiratory endurance, body fat percentage, lean body weight, adverse events profile, and tolerability of the WSE capsules.

RESULTS:

The participant's physical, hematological, and biochemical characteristics were normal, and no significant alterations or irregularities were observed in safety metrics like liver, kidney, and thyroid functions after administering AgeVel®/Witholytin®.

CONCLUSION:

This study found that healthy male participants could consume a standardized WSE at a daily dosage of 1000 mg for four weeks without any adverse effects. Future research should focus on long-term safety assessments in male and female participants.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Ayurveda Integr Med Año: 2024 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Ayurveda Integr Med Año: 2024 Tipo del documento: Article País de afiliación: India