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Efficacy of Manual Therapy in Management of Lumbar disc prolapse

Efficacy of Manual Therapy interventions in Management of Lumbar Prolapsed Intervertebral Disc:A Randomised Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/023037
Enrollment
120
Registered
2020-01-30
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: M511- Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathy

Interventions

Intervention1: Group A: Lumbar traction (15 minutes)
Interferential therapy (15 minutes) and SMWLM for 12 sessions carried out over 4 consecutive weeks. Intervention2: Group B: Lumbar traction (15 minutes)
Interferential therapy (15 minutes) and HVLA grade 5 for 12 sessions carried out over 4 consecutive weeks. Intervention3: Group C: Lumbar traction (15 minutes)
Interferential therapy (15 minutes) and Neural mobilisation for 12 sessions carried out over 4 consecutive weeks. Control Intervention1: Group D: Lumbar traction (15 minutes)
Interferential therapy (15 minutes) for 12 sessions carried out over 4 consecutive weeks.

Sponsors

Guru Jambheshwar University of Science and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with Lumbar PIVD causing Pain, Disability and limited Range of Motion. Unilateral radiating pain to leg below knee. Patient having radiological evidence of PIVD and nerve root compression by MRI

Exclusion criteria

Exclusion criteria: Sequestrated disc Osteoporosis Condition like spondylolisthesis,tumour in lumbar spine Previous history of lumbo-sacral surgery Recent injuries like fractures, grade 3 ligament injuries. Hypermobilty Pregnancy Tuberculosis.

Design outcomes

Primary

MeasureTime frame
Pain Disability SLR ROMTimepoint: all outcome measured before the start of intervention (at 0 weeks) and after the completion of treatment ( at 4 weeks and 6 weeks)

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr Manoj Malik

Guru Jambheshwar University of Science and Technology Hisar

malik_manoj@yahoo.com9896221262

Outcome results

None listed

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