SUTASHEKHARA RASA FOR ORALLY AND BRIHAT JEEVAKADYA TAILA FOR NASAL DROP FOR MIGRAINE

STUDY ON ARDHAVABHEDAKA(MIGRAINE) AND ITS MANAGEMENT WITH BRIHAT JEEVAKADYA TAILA NASYA AND SUTASHEKHARA RASA

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2015/06/005940

Enrollment

Registered

2015-06-22

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- Patients suffering from Ardhavabhedaka

Interventions

Intervention1: In Group A-Brihat jeevakadya Taila Nasya and Sutashekhara Rasa orally: duration-45 days for group A. Nasya 2 sittings for 7 days at the interval of 15 days Control Intervention1: In Gro

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients in the age group 20 to 60 years, presenting with signs and symptoms of Ardhavabhedaka - Migraine described as per Ayurveda and modern science will be included in the study. 2. The diagnosis of the disease shall be done on the basis of clinical manifestations like recurrent attacks of headache, mostly unilateral in site, variable in intensity, frequency and duration with or without nausea, vomiting, aura and GI tract symptoms.

Exclusion criteria

Exclusion criteria: 1. Patients suffering from any chronic debilitating disease, with other neurological pathology, E.N.T. pathology, stress headache and cases which required surgical intervention will be excluded from study. 2. Patients suffering from Sinusitis, Hypertension, Secondary headache caused by meningitis, tumor, encephalitis, cervical spondylitis and refractive errors will be excluded from study. 3. Patients using any other systemic drugs which may alter the results of study. 4. Patients who need psychiatric treatment will be excluded.

Design outcomes

Primary

Measure	Time frame
Improvement will be assessed on the basis of relief found in cardinal symptoms of diseaseProgress in the signs and symptoms based on the standard pattern will be applied before and after treatment.Timepoint: Improvement will be assessed on the basis of relief found in cardinal symptoms of diseaseProgress in the signs and symptoms based on the standard pattern will be applied before and after treatment.	—

Measure

Time frame

Improvement will be assessed on the basis of relief found in cardinal symptoms of diseaseProgress in the signs and symptoms based on the standard pattern will be applied before and after treatment.Timepoint: Improvement will be assessed on the basis of relief found in cardinal symptoms of diseaseProgress in the signs and symptoms based on the standard pattern will be applied before and after treatment.

—

Secondary

Measure	Time frame
Improvement will be assessed on the basis of relief found in cardinal symptoms of diseaseProgress in the signs and symptoms based on the standard pattern will be applied before and after treatment.Timepoint: 45 days	—

Countries

India

Contacts

Public ContactDr D B Vaghela

IPGTRA GAU Jamnagar

drvaghela@rediffmail.com09825407899

Outcome results

None listed

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