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A Clinical trial to study and compare the effects of two drugs,Yastimadhu and Ashwagandha in young patients with Easy Mental Fatiguability.

Evaluation of comparative Clinical efficacy of Yastimadhu Rasayana versus Ashwagandha Rasayana in young adults with symptoms of Easy Mental Fatiguability-A Randomized control trial. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080533
Enrollment
110
Registered
2025-02-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: R538- Other malaise and fatigue

Interventions

None listed

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients who would be ready to accept the treatment protocol guideline as per the study and would give informed consent. All the patients of genders, male and female, of the age group 18 to 30 years, have socioeconomic status in the middle and upper class. Patients belonging to managerial work, student, and academician as an occupation. Patients with symptoms of easy mental fatiguability (Assessed with CIS-R score of more than 26). Patients who are not using any kind of tonics multivitamins for improving general health.

Exclusion criteria

Exclusion criteria: Patients who are not willing to participate in the trial. Patients with Hb levels less than 13 gm% (male) and 9 gm% (female). Patient with acute and chronic Metabolic, Endocrinal, and nutritional disorders. Patients suffering from chronic debilitating diseases. Patients with alcohol and drug abuse. Patients with evidence of delirium, confusion, and other disturbances of consciousness, psychotropic diseases using any psychotropic drug.

Design outcomes

Primary

MeasureTime frame
Mental Fatigue Scores CFS ScoresTimepoint: At the baseline (Day 0) and at the end of intervention (Day 61)

Secondary

MeasureTime frame
MFIS Scores ( to measure the impact of mental fatigue ) FSS Scores ( to assess the severity and frequency) PVT-10 (to assess the overall slowing of Reponses) Satva Scores (Ayurveda) Dhi, Dhriti, Smriti Scores(Ayurveda) VAS-F (subjective assessment of mental fatigue CIS-R Scores (subjective assessment of mental fatigue )Timepoint: At the baseline (Day 0), After one Month (Day 31) and at the end of intervention (Day 61)

Countries

India

Contacts

Public ContactMahima Shrivastava

Mahatma Gandhi Ayurved College, Hospital and Research Centre Salod(H), Wardha,

ayurrulz@gmail.com9403317799

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026