Skip to content

Development of a Simple Blood Analysis Device for Dosha Assessment in Blood

Development of a Device for the Analysis of Blood Obtained via Sira Vedhan for Dosha Assessment in Rakta - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/113074
Enrollment
100
Registered
2026-06-24
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

Parul Institute of Ayurved
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: oPatients within the age range of 18 to 60 years. oPatient with an indication of Siravedhan, e.g.,- Kustha, Rakta pitta, Shula, etc. oPatient giving informed consent.

Exclusion criteria

Exclusion criteria: Age: Below 18 & Above 60 years oPatients who are positive for Hepatitis B, HIV, or VDRL. oPatients who are on Blood thinners (e.g.:-Heparin, Warfarin, Aspirin). oPatients with severe systemic infectious diseases(Hemophilia, Thrombocytopenia , etc.) oPregnant women and Lactating Women. oPatient with low haemoglobin.lower than or equal to 8 gm percent.) o Bedridden Patients. oActive blood donors.

Design outcomes

Primary

MeasureTime frame
Accuracy of the blood analysis device in classifying Dosha predominance in Rakta compared with expert Ayurvedic assessment. Timepoint: Day 1 immediately after Siravedhana and blood analysis

Secondary

MeasureTime frame
Correlation of sensor-derived blood parameters (colour, viscosity, temperature) with Ayurvedic assessment and evaluation of machine-learning-based Dosha classification performance.Timepoint: Time Point: Day 1 (for sensor assessments); Study completion (for machine learning performance analysis).

Countries

India

Contacts

Public ContactDr Harish Daga

Parul Institute of Ayurved

harish.daga26839@paruluniversity.ac.in9413662079

Outcome results

None listed

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