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To evaluate the effectiveness of homoeopathic treatment of Myofascial pain syndrome (pain and spasm in different muscles) of upper back and neck using the Repertory of homoeopathic materia medica by Kent

Effectiveness of homoeopathic treatment of Myofascial pain syndrome of upper back and neck using the Repertory of homoeopathic materia medica by Kent ââ?¬â?? An open label clinical observational study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/042315
Enrollment
40
Registered
2022-04-29
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: M799- Soft tissue disorder, unspecified

Interventions

Intervention1: INDIVIDULAISED HOMOEOPATHIC MEDICINE SELECTED AFTER REPERTORISATION USING HOMOEOPATHIC MATERIA MEDICA BY KENT: Intervention is planned as administering indicated homoeopathic medicines
dosage and repetition depending upon the individual requirement of the cases. Oral medication will be given to each patient for 3 months. Along with medicines, the patients will be advised for physica

Sponsors

NATIONAL INSTITUTE OF HOMOEOPATHY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient fulfilling the clinical diagnostic criteria of Myofascial Pain syndrome (MPS). 2. Age between 15-45 years. 3. Both male and female. 4. Patient willing to take part in the study and given written consent in English/Hindi/Bengali for the same. In a case of minor, signature will also be taken from the legal guardian in the form.

Exclusion criteria

Exclusion criteria: 1. Patients with local or systemic infection, patients with acute muscle, or bony trauma. 2. Patient on any life supporting drugs. 3. Patient with serious comorbidities. 4. Pregnant or lactating females. 5. Currently receiving homoeopathic treatment for any chronic condition(s). 6. Substance abuse and/or dependence.

Design outcomes

Primary

MeasureTime frame
Reduction in intensity of pain and disability measured by Copenhagen Neck Functional Disability Scale.Timepoint: Baseline and 3rd month

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactAMITAVA SAMANTA

National Institute of Homoeopathy

samanta.amitava1@gmail.com9433485138

Outcome results

None listed

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