To study the effect of panchbhautika nasal drops in the patients with migraine

An open labelled randomized comparative clinical study to evaluate the efficacy of panchbhautika nasal drops in the management of ardhavabhedaka with special reference to migraine - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/084946

Enrollment

Registered

2025-04-16

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-28

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

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients will be enrolled in the study based on the diagnostic criteria for ardhavabhedaka migraine 2. Patients will be selected from 18-60 years Age group 3. Patients who will be fit for Pratimarsh Nasya karma

Exclusion criteria

Exclusion criteria: 1. Patients of ardhavabhedaka migraine who are taking alternative medicines 2. Other known case of any systemic disease HTN COPD etc 3. Patients with conditions such as brain tumors meningitis cervical spondylitis encephalitis referred pain refractive errors or glaucoma will not be enrolled in this study 4. Contraindicated for nasal instillation Pratimarsh Nasya karma

Design outcomes

Primary

Measure	Time frame
To Evaluate the Efficacy of Panchbhautika nasal drops in The Management of Ardhavabhedaka with Special reference to MigraineTimepoint: At baseline on 15th day 30th day 45th day 60th day 75th day and 90th day	—

Secondary

Measure	Time frame
relief from symptoms of migraineTimepoint: 90 days	—

Countries

India

Contacts

Public ContactDr Manjiri keskar

Parul Institute of Ayurveda

manjirikeskar@gmail.com9822606358

Outcome results