Masha taila nasya in tension type headache

A randomized open labelled controlled clinical study to evaluate the efficacy of masha taila nasya in the management of vataja shirashoola with special reference to Tension type headache

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/08/044734

Enrollment

Registered

2022-08-17

Start date

Unknown

Completion date

Unknown

Last updated

2022-10-17

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

Conditions

Health Condition 1: G442- Tension-type headache

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subjects within the age of 21Ã¢â?¬â??40-year-old 2.Subject full filling diagnostic criteria 3.Subjects willing to sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Subjects taking any antipsychotic drugs 2.Subjects having any other chronic systemic illness 3.Subjects having nausea/ vomiting 4.Subject contra-indicated for Nasya

Design outcomes

Primary

Measure	Time frame
Changes in Vataja shiroroga after the treatment VISUAL ANALOGUE SCALETimepoint: 0th day - Before treatment 8th day - After treatment 15th day - 1st follow up 30th day - 2nd follow up	—

Secondary

Measure	Time frame
. Tivra nisi atimatra shiroruja (Pain aggravates in the night) 2. Shankha nisthudyathe (Bitemporal head ache) 3. Ghata pradesha nistudyate brusham (Pain in the occipital region) 4. Bhruvormadhyam lalata cha patativa ativedana (Severe pain in the forehead) Timepoint: 0th day - Before treatment 8th day - After treatment 15th day - 1st follow up 30th day - 2nd follow up	—

Countries

India

Contacts

Public ContactDr Aswathy P

Sri Sri College of Ayurvedic Science and Research Hospital

ayurgeeta@gmail.com9480056218

Outcome results