Skip to content

â??A Clinical Study on Swarnaprashan to Establish its Safety in children suffering from recurrent infections"

â??An Experimental and Clinical Study on Swarnaprashan to Establish its Safety, antimicrobial activity and to Assess its Immunogenicity Effect after BCG Vaccinationâ??

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036941
Enrollment
50
Registered
2021-09-29
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: J06- Acute upper respiratory infectionsof multiple and unspecified sites

Interventions

Intervention1: â??An Experimental and Clinical Study on Swarnaprashan to Establish its Safety, antimicrobial activity and to Assess its Immunogenicity Effect after BCG Vaccinationâ??: It will be a sin
S.S. Hospital, IMS, BHU after assessing the following exclusion and inclusion criteria - Intervention2: An Experimental and Clinical Study on Swarnaprashan to Establish its Safety, antimicrobial acti
S.S. Hospital, IMS, BHU after assessing the following exclusion and inclusion criteria - dURATION OF STUDY -3 MONTHS Control Intervention1: SWARNAPRASHAN: After confirming the non-toxic effects of Sw

Sponsors

INSTITUTE OF MEDICAL SCIENCES BANARAS HINDU UNIVERSITY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a) Age between 1to 15 years b) Having history of repeated respiratory or any other recurrent disorder irrespective to associated congenital, hereditary or developmental/nutritional disorders c) Period of drug administration - asymptomatic Phase

Exclusion criteria

Exclusion criteria: a) Neonates and infants b) During any symptomatic illness c) Suffering from degenerative neurological, IEM, etc.

Design outcomes

Primary

MeasureTime frame
IMPROVEMENT IN immunity and overall health condition due to reduction in number of episodes of illness and safety of drugTimepoint: after one month of administration of drug

Secondary

MeasureTime frame
IMPROVEMENT IN immunity and overall health condition due to reduction in number of episodes of illnessTimepoint: after 2months of follow up

Countries

India

Contacts

Public ContactDR SAHANA SHANKARI

INSTITUTE OF MEDICAL SCIENCE BHU VARANASI

hodkb2006@yahoo.in7355644462

Outcome results

None listed

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