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Clinical evaluation of efficacy of Rasnadashamoola kwatha in the management of Ardhavabhedhaka(Migraine).

A Randomized controlled clinical study to evaluate the efficacy of Rasnadashamoola kwatha over Pathyadi kwatha in the management of Ardhavabhedhaka (Migraine) - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080644
Enrollment
40
Registered
2025-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: G439- Migraine, unspecified

Interventions

None listed

Sponsors

DR SAMPREETA A S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Subjects aged between 16-60 years of either gender. 2 Subjects fulfilling the Diagnostic criteria of Ardhavabhedaka (Migraine) 3 Subjects of Migraine without Aura. 4 Both Fresh and treated cases will be considered for study. 5 Subjects who are willing to sign the Consent.

Exclusion criteria

Exclusion criteria: 1 Diagnosed cases of Anantavata (Trigeminal Neuralgia), Suryavartha, Dustapratishyaya (Chronic Sinusitis). 2 Subjects having a history of severe head injury. 3 Subjects with known systemic disorders [like- Uncontrolled hypertension, Cardiac problems] which interfere the intervention of Study. 4 Known cases of psychological disorder. 5 Subjects of Migraine with Aura 6 Any other illness which the researcher feels that interferes the intervention of study.

Design outcomes

Primary

MeasureTime frame
Effect of Trial drug on improvement in classical symptoms of Ardhavabhedaka (Migraine)Timepoint: 7day,15day,30day

Secondary

MeasureTime frame
Safety of the trial drug and adverse drug reaction and aggravation in the symptoms of Ardhavabhedaka (Migraine)Timepoint: 7day,15day,30day

Countries

India

Contacts

Public ContactDR SAMPREETA A S

Sidramappa Danigond Memorial Trusts Ayurvedic Medical College Post Graduation Centre

vaidyasukumar@gmail.com9986125625

Outcome results

None listed

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