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A clinical study to see the effect of some Ayurvedic formulations in the management of Mental Retardation.

Phase 2
Conditions
Health Condition 1: null- Cognitive Deficit
Registration Number
CTRI/2012/03/002536
Lead Sponsor
Central Council for Research in Ayurvedic Sciences CCRAS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
150
Inclusion Criteria

1. Children with Intelligence Quotient 70 - 84 (Weschlerâ??s-IQ Indian adaptation by Malin)

2. Willing and able to participate for 16 weeks. (Assent to be obtained from Parent(s) / Guardian(s)).

Exclusion Criteria

1. Children suffering from major systemic illness necessitating long term drug treatment.

2. Children with evidence of malignancy.

3. Children 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. H/o hypersensitivity to any of the trial drug or their ingredients

5. Children who have completed participation in any other clinical trial during the past six (06) months.

6. Any other condition which the P.I. thinks may jeopardize the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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