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Effect of Uraimathirai in Increasing children Immunity

Evaluation of Clinical efficacy of Uraimathirai as Immunomodulator

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/06/008723
Enrollment
60
Registered
2017-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Intervention1: URAI MATHIRAI: 50 MG DAILY UPTO SIX MONTHS Control Intervention1: THALEESATHI CHOORANAM: 1 GRAM TWICE DAILY FOR SIX MONTHS

Sponsors

CENTRAL COUNCIL FOR RESEARCH IN SIDDHA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children of either gender aged 6 MONTHS to 6 Years with a history of recurrent URTIs and presenting with URTI at hospital treatment. �  The definition used for recurrent URTIs was three or more such episodes during the last 12 months. �  The current episode required for study eligibility was Defined by the presence of at least two of the following Rhinitis Pharyngitis cough hoarseness, Temperature More than 38.5�°C, Prescription of an antibiotic for a URTI, occurring after an asymptomatic Period of at least 1 week without antibiotics

Exclusion criteria

Exclusion criteria: occurrence of otitis media and/or sinusitis and/or infection of the lower respiratory tract (ie, bronchitis, pneumonia)and/or proven group A streptococcal angina at the enrollment Further main exclusion criteria were allergic asthma, significant systemic disease (eg, hepatic and/or renal disease, malignancy), immune system disorders, suspected Malabsorption, major surgical procedure within 3 months of commencement of the study recent immunosuppressive or immunostimulant therapy, or corticosteroids.

Design outcomes

Primary

MeasureTime frame
Reduction in Recurrence of Resp Infections Clinical Improvement No Antibiotic treatment Increase in Anti bodies IgA/IgG Decrease in Phagocytosis Timepoint: 6 months

Secondary

MeasureTime frame
Safety of trial drugTimepoint: 6 months

Countries

India

Contacts

Public ContactDRPSATHIYARAJESWARAN

SIDDHA CENTRAL RESEARCH INSTITUTE

siddha2k6@gmail.com04426214809

Outcome results

None listed

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