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Bioavailability of four ayurvedic polyherbal formulations

Evaluation of bioavailability of four Ayurvedic poly-herbal formulations in healthy volunteers – A Cross over Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/044447
Enrollment
6
Registered
2022-07-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

None listed

Interventions

None listed

Sponsors

Ministry of AYUSH Govt of India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Apparently healthy subjects free from any known disease. 2. Volunteers with their vitals in normal range, normal Liver Function Test (LFT) and Kidney Function Test (KFT) values. 3. All gender categories 4. Age group of 18-70 years. 5. Subjects who agree to participate in the study and give their full consent.

Exclusion criteria

Exclusion criteria: 1. Volunteers who deny to give consent for the study. 2. Volunteers whose vitals, LFT and KFT values are not under normal limits. 3. Pregnant / Lactating women. 4. Subjects taking any form of treatment for any illness 5. Any other condition which the investigator thinks may jeopardize the safety of the subject.

Design outcomes

Primary

MeasureTime frame
Estimation of time taken by each formulation to reach maximum concentration in the systemic circulation.Timepoint: 0.5hr, 1hr, 2hr, 4hr, 6hr, 12hr, 24hr post administration of drug—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactDr Sharada Anand

Central Ayurveda Research Institute

dr.shaaradaramesh@gmail.com9620554829

Outcome results

None listed

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