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To Evaluate Efficacy of Migreez Tablets and Drops in patient suffering from chronic migrain

Open labelled Prospective Randomized single Arm clinical trial to Evaluate the efficacy and safety of Migreez Tablet and nasal drop in management of Chronic Migrain - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092614
Enrollment
35
Registered
2025-08-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: G00-G99- Diseases of the nervous system

Interventions

None listed

Sponsors

Vedistry Pvt. Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects with having with symptoms of Migraine one sided throbbing headache /Nausea & vomiting Sensitivity to light & sound more than 3 months Completed the screening process within 3 days prior to randomization Study participant has understood and signed the informed consent form to participate in the study. Study participant willing to be available for the entire study period and adhere to protocol requirements as evidenced by signing the informed consent document

Exclusion criteria

Exclusion criteria: Complicated and special types of gastritis hemorrhage peptic ulcer cholelithiasis cholecystitis, dysplasia of gastric mucosa or pathological diagnosis of suspected malignant change Reports any presence or history of a clinically significant disorder involving the cardiovascular, respiratory, renal, urologic, hepatic, immunologic, endocrine, or neurologic systems or psychiatric disease as determined by the investigator(s). Pregnant and lactating women; Had a history of allergy from trial medication; Subject who has been involved with another experimental trial within the past 30 days from the date of recruitment. Subjects using over-the-counter or prescription anti-reflux agents (Allopathic, Herbal, Homeopathic, Ayurveda, Unani, Siddha medicines) within the past 14 days from the date of recruitment.

Design outcomes

Primary

MeasureTime frame
1.Reduction in migraine pain intensity over 30 days by a validated pain scale 2.Decrease in the number of migraine episodes per week over 30 days 3.Reduction in the occurrence of nausea, vomiting, photophobia, and phono phobia over 30 days 4.Time to significant relief from acute migraine pain over 30 daysTimepoint: 1 Visit 1 Baseline 2 Visit 2 Day 15 3 Visit 3 Day 30

Secondary

MeasureTime frame
Safety of Migreez Tablet & Drop in chronic migraine patients.Timepoint: 1 Visit 1 Baseline 2 Visit 2 Day 15 3 Visit 3 Day 30

Countries

India

Contacts

Public ContactDr T vishala

Yashwant Ayurvedic College

drmanasimaurya@vedistry.com9619528619

Outcome results

None listed

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