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Amalakavleha as Rasayana in healthy individuals

A clinical study to evaluate the efficacy of Amalakavleha as Rasayana in healthy individuals

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021387
Enrollment
20
Registered
2019-09-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Amalakavleha: 10 grams Once a day (In morning) orally for 8 weeks duration Reference - Ch. Chi. 1/2/7 Control Intervention1: Starch capsules: 500 mg once a day (in morning) for 8 weeks

Sponsors

Principal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy individuals willing to undergo trial 2. Individuals ready to give written consent 3. Healthy volunteers of either sex aged between 30 to 60 years 4. Individuals willing and able to participate for 8 weeks duration

Exclusion criteria

Exclusion criteria: 1. Individuals not willing to undergo trial 2. Individuals below 30 years and above 60 years of age 3. History of hypersensitivity towards trial drug or its ingredients 4. Individuals who have participated in any other clinical trial during past 6 months

Design outcomes

Primary

MeasureTime frame
Fulfillment of objective and subjective criteriaTimepoint: 8 weeks

Secondary

MeasureTime frame
General feeling of well beingTimepoint: 8 Weeks

Countries

India

Contacts

Public ContactPriyankisha

RGGPG Ayurvedic college and hospital Paprola

drvijaychaudhary@gmail.com9418130228

Outcome results

None listed

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