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A clinical trial of natrum muriaticum in centesimal potencies versus individualized homoeopathic medicine in chronic migraine

Comparative study of physicochemical profiles of natrum muriaticum 3x trituration and tablet prepared manually and mechanically and a pilot open-label non-randomized clinical trial of natrum muriaticum in centesimal potencies versus individualized homoeopathy in chronic migraine - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102358
Enrollment
40
Registered
2026-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: G437- Chronic migraine without aura

Interventions

Intervention1: Natrium muriaticum in centesimal potency: Medicine will be prescribed at baseline and followed up each month for next three months Control Intervention1: Individualized Homoeopathic Med

Sponsors

Subhashree Modak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged between 18 and 60 years. A clinical diagnosis of chronic migraine, defined as headache occurring on 15 or more days per month for a duration of at least three consecutive months. On at least 8 days/month, the headache should fulfill criteria for migraine without aura (1.1), or respond to migraine-specific treatment (e.g., triptans, ergot derivatives)., in accordance with the International Classification of Headache Disorders, 3rd edition (ICHD-3). MIDAS score is greater than or equal to 6. Willingness to provide written informed consent and comply with study procedures. Not taking any other homeopathic treatment during the study period. Willing to report and refrain from starting new allopathic or alternative interventions for migraine during the study.

Exclusion criteria

Exclusion criteria: Presence of a secondary headache disorder (e.g., attributed to trauma, vascular disorders, intracranial neoplasms, infections, substance use/withdrawal, or psychiatric illness, as defined by ICHD-3 (e.g., code 6 12). Other Primary Headache Disorders: Diagnosed with cluster headache, chronic tension-type headache without migraine features, medication overuse headache, or hemiplegic/basilar migraine. Severe Uncontrolled Comorbidities: Uncontrolled hypertension, diabetes mellitus, renal, hepatic, or cardiac diseases that may interfere with study outcomes. Coexisting severe psychiatric conditions (such as History of major depression, bipolar disorder, or schizophrenia etc.) that may interfere with assessment. Pregnancy or lactation. Use of ongoing prophylactic headache medication that cannot be safely discontinued. Unwillingness to adhere to study protocol or provide written informed consent. Concurrent enrollment in another clinical trial within the last 3 months.

Design outcomes

Primary

MeasureTime frame
Migraine Disability Assessment Scale (MIDAS) to assess impact on daily functioningTimepoint: At baseline and three months

Secondary

MeasureTime frame
Visual Analogue Scale (VAS) for headache intensity. Frequency of chronic headache attacks (monthly).Timepoint: At baseline and three months

Countries

India

Contacts

Public ContactProf Dr Kaushik Deb Das

The Culcutta Homoeopathic Medical College and Hospital

drkaushikddas25@gmail.com9932298682

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026