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A clinical study to evaluate the effectiveness of Pancharavinda Vati and Tungadrumadi Taila Nasya in children with Attention Defecit Hyperactive Disorder.

To evaluate the Combined Effectiveness of Pancharavinda Vati and Pratimarsha Nasya with Tungadrumadi Taila on Attention Defecit Hyperactivity Disorder in Children- An open label clinical trial

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/053167
Enrollment
30
Registered
2023-05-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F01-F99- Mental, Behavioral and Neurodevelopmental disorders

Interventions

None listed

Sponsors

DR AJAY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: children of age group 6 to 15 years fullfilling the Diagnostic criteria of ADHD irrespective of gender,religion and socioeconomic status

Exclusion criteria

Exclusion criteria: 1.ADHD children with other neurological complaints such as seizures, bipolar mode disorder, autistic spectrum disorder. 2. Children suffering from chronic illness, developmental disorder and other congenital disorders/neurobehavioral disorders and mild to severe mental retardation will be excluded.

Design outcomes

Primary

MeasureTime frame
Changes in scores of assessment scale of ADHDTimepoint: baseline to endpoint assessment

Secondary

MeasureTime frame
conceptual study of ADHD in children vis-a-vis Unmada contemplating both Ayurveda and modern point of view .Timepoint: Baseline,30th day ,60th day.

Countries

India

Contacts

Public ContactDr Ajay

SDM Institute of Ayurveda and Hospital Anchepalya Bengaluru

drgirishkumargowda@gmail.com9449577136

Outcome results

None listed

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