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Homeopathy for neck pain

A double-blind, randomized, placebo-controlled trial of individualized homoeopathic medicines in managing neck disability in cervical spondylosis in adults - NIL

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092902
Enrollment
126
Registered
2025-08-12
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: M479- Spondylosis, unspecified

Interventions

Intervention1: Individualized Homoeopathic Medicines: IHMs will be used to treat the recruited individuals with cervical spondylosis.According to the situation or condition, the intervention will invo
these situations will be compared between groups.Therapeutic exercises include Isometric exercise - Cervical flexion, Cervical extension, Right Lateral Flexion, Left Lateral Flexion, Right Rotation

Sponsors

D N De Homoeopathic Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient with age group 18-65 yrs. 1.Participants of either sex or transgender. 2.Patient suffering from Cervical Spondylosis verified by clinical examination as well as X ray findings. 3.Patient with mild to moderate neck pain. according to NDI score 5-24

Exclusion criteria

Exclusion criteria: 1.Not providing with written informed consent of participation. 2.Severe degeneration of Cervical Spine with marked degeneration of vertebrae, having neck trauma/fracture/history of surgery/congenital spinal abnormalities, any systemic disease of bones and joints and other non- specific neck pain lesion. 3.Non-ambulant patients. 4.Immune compromised state. 5.Substance abuse or dependence 6.Too unwell to take part. 7.Patient with unstable psychiatric disorder. 8.Pregnancy and puerperal and Lactating women. 9.Patient with severe neck pain. 10.Undergoing homoeopathic treatment for any chronic disease within last 6 months. 11.Simultaneous participation in any other clinical trial.

Design outcomes

Primary

MeasureTime frame
Neck Disability Index (NDI)Timepoint: Baseline, and every month, up to 3 months

Secondary

MeasureTime frame
Pain 0-10 Numerical Rating Scale (NRS)Timepoint: Baseline, and every month, up to 3 months;Measure Yourself Medical Outcome Profile version 2 (MYMOP-2)Timepoint: Baseline, and every month, up to 3 months

Countries

India

Contacts

Public ContactProf Dr Arpita Basu

D N De Homoeopathic Medical College and Hospital

sayani2659@gmail.com9332612659

Outcome results

None listed

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