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To see effectiveness of various non-operative treatment in patient suffering from disc prolapse in spinal column of lumbar

To evaluate the effectiveness of conservative treatment in patients with lumbar disc prolapse - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/04/085431
Enrollment
200
Registered
2025-04-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: S342- Injury of nerve root of lumbar andsacral spine

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil

Sponsors

Stavya Spine Hospital and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age 18 and 60 years. 2.Presence of lower back pain and radicular symptoms of a minimum duration of 1 month. 3.Diagnosis of lumbar disc prolapse with associated nerve root compression, as confirmed by magnetic resonance imaging , corresponding to the clinical presentation of radicular symptoms.

Exclusion criteria

Exclusion criteria: 1.Presence of neurological deficit. 2.A documented history of prior lumbar spine surgery. 3.Patients presenting with significant neurological deficits e.g., severe muscle weakness or cauda equina syndrome requiring immediate surgical intervention. 4.Patients with a history of neuropsychiatric conditions. 5.Individuals with a history of traumatic injury to the lumbar spine. 6.Individuals with significant comorbidities that may interfere with treatment outcomes e.g., severe osteoporosis, malignancies, or systemic inflammatory disorders.

Design outcomes

Primary

MeasureTime frame
1.To conduct a comprehensive clinical evaluation of the enrolled patients, documenting relevant data at subsequent follow-up intervals of 3 months, 6 months, and 1 year 2.To quantitatively assess the degree of pain relief reported by patients during each follow-up visit. 3.To evaluate improvements in functional outcomes over the course of the follow-up visits.Timepoint: Visits at 3 months,6 months and 12 months

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Bharat R Dave

Stavya Spine Hospital And Research Institute

brd_172@yahoo.com09825019913

Outcome results

None listed

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