Skip to content

Homeopathic treatment for chronic low back pain in adults

An exploratory, open-label, randomized, controlled, pilot trial comparing the effects of individualized homoeopathic medicines in LM potencies with centesimal potencies in managing chronic low back pain in adults - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/093971
Enrollment
102
Registered
2025-09-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: M545- Low back pain

Interventions

Intervention1: Individualized homoeopathic medicines in LM potencies plus concomitant care: The enrolled patients of chronic low back pain will be treated with individual homoeopathic medicines (IHMs)
dosage and repetition depending upon the individual recruitment of the cases. Patients will be advised to refrain from handling the bottle or from eating, drinking, smoking or brushing teeth within 30

Sponsors

D N De Homoeopathic Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age group 18-65 years 2. Participants of either sex or transgender 3. Patients suffering from low back pain for 3months or more 4. Patients suffering from moderate and severe pain; using Numeric Rating Scale (NRS).Patients will be categorized into mild (NRS 0-3), moderate (NRS 4-7) or severe (NRS 8-10). 5. Patients with radiological diagnosis indicating different causes of low back pain, mild to moderate degenerative radiological changes.

Exclusion criteria

Exclusion criteria: 1. Unwilling to take part and not providing with written informed consent of participation. 2. Patients who have undergone spine surgery within 6 months. 3. Patients with severe degenerative changes in radiological findings like congenital abnormalities, infection, tumour, malignancy. 4. Patients having severe and extremely severe DASS-21 score (severe depression-11-13, anxiety-8-9, stress-13-16 and extremely severe depression-14+, anxiety -10+, stress-17+) 5. Immuno-compromised state, AIDS, hepatitis et 6. Uncontrolled diabetes, hypertension, cancer or any other systemic illness or any vital organ failure. 7. Vulnerable population: unconscious,non-ambulatory,too sick for consultation, differently abled, terminally or critically ill patients, mentally incompetent people. 8. Tobacco chewing and/ or smoking, alcoholism and/ or any form(s) of substance abuse and/ or dependance (TAPS tool) 9. Pregnancy, puerperal women and lactating mother. 10. Undergoing homoeopathic treatment for any chronic disease within last 6months. 11. Simultaneous participation in any other clinical trial.

Design outcomes

Primary

MeasureTime frame
To explore feasibility of a definitive future trialTimepoint: 3 months

Secondary

MeasureTime frame
Oswestry Disability Index (ODI)Timepoint: Baseline, every month, up to 3 months;Depression, Anxiety, Stress Scale Short Form (DASS-21)Timepoint: Baseline, every month, up to 3 months

Countries

India

Contacts

Public ContactSubhasish Ganguly

D N De Homoeopathic Medical College and Hospital

deepsikha.9201@gmail.com8250157886

Outcome results

None listed

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