Clinical efficacy and safety of Isha Balm

Not Applicable

Not yet recruiting

• Conditions: Headache

• Registration Number: CTRI/2018/02/011819
• Lead Sponsor: Isha Arogya pvt ltd

Brief Summary

This study a single arm study among the outpatient attending the clinic. To study the safety and therapeutic efficacy of indigenous herbal formulation of Isha Arogya namely Isha Balm  topical application used as a supportive theraphy among patients presenting with headache and nasal symptoms. 30 patients for the period of 15 days.

Detailed Description

Not available

Study Timeline

• Study Start: 2018-02-20
• Last Update Posted: 2018-08-02

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

1Patients attending the clinic in the age group of 12 years and above and both the sexes included 2 Patients provisionally diagnosed to have viral prodrome, common cold, acute sinusitis, tension headache, migraine headache with the symptom of headache are included the study with their consent.

Exclusion Criteria

• 1 past medical records needing neurological evaluation for headache 2known cases of hypertention, and those getting treatment complications of uncontrolled hypertention 3having ophthalmic complaints 4Patients with serious co-morbid illnesses such as known cardiac vascular disease, cancer induced pain, injuries due to fall or accidents, systemic illness like SLE,etc •Patients below the age of 12 years and above 60 years.
• •Patients who are not willing to give informed written consent.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Relief from headache	3 days

Secondary Outcome Measures

Name	Time	Method
Relief from Nasal block	3 days

Trial Locations

Locations (1)

Isha Arogya Health Centre chennai; 🇮🇳 Chennai, TAMIL NADU, India

Isha Arogya Health Centre chennai

🇮🇳Chennai, TAMIL NADU, India

Dr S Keerthiga

Principal investigator

9442590085

keerthiga.black@gmail.com