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Pharmacokinetics of Amrtottaram Kashayam in Healthy Volounteers: A Pilot Study

Pharmacokinetics of Amrtottaram Kashayam through Metabolomic Profiling using LC-MS/MS: A Pilot Study - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100842
Enrollment
1
Registered
2026-01-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Madhu K P
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy volounteers with no history of cardiac, hepatic, renal, haematological, psychiatric illness. Normal lab values of CBC, RFT, LFT, Blood sugar. Not under any medication or supplementation for at least two weeks before the study. Non smokers and Non-alcoholics

Exclusion criteria

Exclusion criteria: Pregnant women, Lactating mothers, infection or fever in the last two weeks, History of Diabetes Mellitus, Hypertension, Dyslipidaemia, Hyper and Hypothyroidism, Recent vaccinations within one month

Design outcomes

Primary

MeasureTime frame
Metabolomic profile of Blood plasma obtained by LC-MS/MS at different time intervalsTimepoint: 0th Hour, 30 minutes, 1st, 2nd, 4th, 8th, 12th, 24th and 48th hours—

Secondary

MeasureTime frame
Metabolomic profile of Urine sample obtained by LC-MS/MS at different time intervalsTimepoint: 0-2, 2-4, 4-8, 8-12 hours—

Countries

India

Contacts

Public ContactMadhu K P

Vaidyaratnam P S Varier Ayurveda College

madhusukrutham@gmail.com9745994515

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026