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To study the effectiveness of three ayurvedic drug combination in common cold in children.

A comparative clinical study of Amrita, shrish, kantkari syrup in pratishyaya w.s.r to Common cold in children.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031010
Enrollment
30
Registered
2021-02-04
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

Health Condition 1: J00- Acute nasopharyngitis [common cold]

Interventions

Intervention1: amrita shrish kantkari: Group A- This group of children will be given the trial drug Amrita, Shirish, Kantkari syrup orally for 20 days. According to need it may be increase for 10day

Sponsors

Dr Mahesh Narayan Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Physical examination & clinically significant abnormal lab investigation at pre study. 2.Having allergy history. 3.Who fulfill diagnostic criteria of pratishyaya

Exclusion criteria

Exclusion criteria: 1.Below 2yrs & above 16 yrs 2.Congenital defects & disorders 3.Having severe cardiovascular,gastrointestinal & renal disease. 4.Hematological, Neurological & psychiatric disease.

Design outcomes

Primary

MeasureTime frame
DIGNOSTIC CRITERIA- 1. Nasal blockage 2. Kadu nasa,netra,gala,talu 3. Shiro gurutva 4. Fever 5. Sneezing 6. Swarabheda 7. Cough 8. Lacrimation 9. Runny nose 10. Sore throat We select the patient if he/she present the minimum five criteria positive. Timepoint: The observation of patients will be carried out during the trial at every 5 days interval for 20 days and after completion of trial 15 days interval. Both objective and subjective parameters as per requirement will be taken. Next follow up should be taken at 45 days for assesment of recovery.—

Secondary

MeasureTime frame
DIGNOSTIC CRITERIA- 1. Nasal blockage 2. Kadu nasa,netra,gala,talu 3. Shiro gurutva 4. Fever 5. Sneezing 6. Swarabheda 7. Cough 8. Lacrimation 9. Runny nose 10. Sore throat We select the patient if he/she present the minimum five criteria positive. Timepoint: The observation of patients will be carried out during the trial at every 7days interval for 20 days and after completion of trial 15 days interval. Both objective and subjective parameters as per requirement will be taken. Next follow up should be taken at 45 days for assesment of recovery.—

Countries

India

Contacts

Public ContactPooja Tomer

State ayurvedic college lkw

mngupta75@yahoo.com9415447523

Outcome results

None listed

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