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Homoeopathic Treatment Of Chronic Lower Back Pain (Lumbar Spondylosis)

Utility Of Kents Repertory In Selection Of Individualized Homoeopathic Medicine For Management Of Lumbar Spondylosis- A Prospective Single Arm, Open Label Clinical Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067157
Enrollment
30
Registered
2024-05-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: M478- Other spondylosis

Interventions

Intervention1: Individualized Homoeopathic Medicine After Repertorization Done Using Repertory Of Homoeopathic Material Medica By J.T.Kent: Patients qualifying to inclusion criteria will be included i

Sponsors

State National Homoeopathic Medical College And Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Duration of back pain should be at least 3 months. 2. Patient giving consent to participate. 3. Patient having no other complicated systemic disease. 4. Patient presenting with non- traumatic back pain. 5. In cases, where patients are already taking Homoeopathic medicine for lumbar spondylosis will be taken up for studies only after a wash out period of two weeks.

Exclusion criteria

Exclusion criteria: 1. Patient presenting with traumatic back pain. 2. Cases already taking Homoeopathic treatment for any other systemic illness. 3. Patient who were not willing to come for follow up. 4. Patients having any serious medical illness. 5. Pregnant women and lactating mothers.

Design outcomes

Primary

MeasureTime frame
Quebec Back Pain Disability Questionnair (QBPD). This scale is a 20- item self administered questionnaire designed to assess the level of functional disability in individuals with back pain. Add up the selected numbers for a total score. The minimum score is 20 and the maximum score is 100. Higher scores correlate to greater disability. Timepoint: Outcome will be assessed initially at the baseline 4 weeks interval up to 6 months.—

Secondary

MeasureTime frame
Visual Analogue scale (VAS) for pain and stiffness is a scale of 0 to 100 mm (“0 ? score indicate no pain and no stiffness, whereas "100" mm indicates worst pain and worst stiffness possible, before and after treatment)Timepoint: Outcome will be assessed initially at the baseline 4 weeks interval up to 6 months.—

Countries

India

Contacts

Public ContactDr Rituraj

State National Homoeopathic Medical College And Hospital, Lucknow

drnutansharma@gmail.com8178562292

Outcome results

None listed

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