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Clinical Trials/CTRI/2018/05/013661
CTRI/2018/05/013661
Not yet recruiting
Phase 2

Study of Morbidity Status of Children and the Effect of Abhaya Ghrita on Lowering Down the Morbidity Rate

ational Institute of Ayurveda Jaipur0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: null- 1 Children with recurrent respiratory infections. 2 Children with recurrent G.I.T. diseases.3 Children with recurrent fever.4 Children with other recurrent diseases

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: null- 1 Children with recurrent respiratory infections. 2 Children with recurrent G.I.T. diseases.3 Children with recurrent fever.4 Children with other recurrent diseases
Sponsor
ational Institute of Ayurveda Jaipur
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
ational Institute of Ayurveda Jaipur

Eligibility Criteria

Inclusion Criteria

  • •1\. Children aged from 06 months to 05years of either sex.
  • •2\. Children with recurrent respiratory infections.
  • •3\. Children with recurrent G.I.T. diseases.
  • •4\. Children with recurrent fever.
  • •5\. Children with other recurrent diseases

Exclusion Criteria

  • •1\. Subjects suffering from major systemic illness necessitating long term treatment.
  • •2\. Subjects with evidence of malignancy.
  • •3\. Subjects with concurrent serious hepatic dysfunction (defined as AST and/or ALT \>3 times of the upper normal limit) or renal dysfunction (defined as S.creatinine \>1\.2mg/dl), uncontrolled pulmonary dysfunction (asthmatic and COPD patients)
  • •4\. Co\-morbidity like TB, UTI and bleeding disorders etc.
  • •5\. H/o hypersensitivity to any of the trial drug or their ingredients.
  • •6\. Subjects who have completed participation in any other clinical trial during
  • •the past six months.

Outcomes

Primary Outcomes

Not specified

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