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EFFICACY OF PATHYADI CHOORNA IN KAPHAJA KASA IN CHILDREN

A randomized controlled clinical trial to evaluate the efficacy of Pathyadi choorna in Kaphaja Kasa in children. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059707
Enrollment
114
Registered
2023-11-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: J069- Acute upper respiratory infection,unspecified

Interventions

None listed

Sponsors

SREERAJ R
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Children with Pratyatma lakshana of Kaphaja Kasa 2) Patients having Kasa less than 10 days will be selected 3)Patient with a minimum of any two symptoms other than Kaphaja Kasa

Exclusion criteria

Exclusion criteria: 1) All Kasa other than Kaphaja are excluded 2) Patients with history of malignancy or any other congenital anatomical abnormalities of chest and respiratory system, K/C/O Pneumonia, Croup syndrome, K/C/O Congenital Anomalies and patients of Chronic obstructive bronchitis, Pleurisy, Pulmonary tuberculosis, Lung abscess and Astma will be excluded

Design outcomes

Primary

MeasureTime frame
BLOOD EXAMINATION 1) Haemoglobin Estimation (HB%) 2) Total Leukocyte Count (TLC) 3) Differential count (DC) 4) Erythrocyte Sedimentation Rate (ESR) 5) Absolute Eosinophil Count (AEC)Timepoint: baseline, and on 10th day

Secondary

MeasureTime frame
Changes in values of the following on any other day other than baseline & 10th day BLOOD EXAMINATION 1) Haemoglobin Estimation (HB%) 2) Total Leukocyte Count (TLC) 3) Differential count (DC) 4) Erythrocyte Sedimentation Rate (ESR) 5) Absolute Eosinophil Count (AEC)Timepoint: baseline & 10th day

Countries

India

Contacts

Public ContactSreeraj R

PDEA College of Ayurveda

drdeodasms@gmail.com9423010818

Outcome results

None listed

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