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Post operative pain relief in lumber spine surgery patients

Comparison of the post operative analgesia after epidural application of gel foam soaked in morphine ropivacaine and morphine ropivacaine combination in patients undergoing single level lumbar laminectomy a randomised controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055003
Enrollment
75
Registered
2023-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system Health Condition 2: M512- Other thoracic, thoracolumbar andlumbosacral intervertebral disc displacement

Interventions

Intervention1: Morphine: Gelfoam soaked in inj morphine 5 mg (0.5 ml) + 10 ml of 0.9% sodium chloride in epidural space Intervention2: Ropivacaine: Gelfoam soaked in 10 mL of 0.5% ropivacaine + 0.5 ml

Sponsors

M D M Hospital Dr S N Medical College Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I /II scheduled to undergo single-level lumbar laminectomy under general anaesthesia

Exclusion criteria

Exclusion criteria: 1 Body mass index >= 25 kg/m2 2 Moderate to severe heart or lung disease 3 History of previous lumbar spinal surgery 4 Prior neurological disease 5 Prior neuromuscular disease or psychological disease 6 History of preoperative opioid use or any history of substance abuse or on steroids 7 History of allergic reactions to local anesthetics. 8 Patients with excessive bleeding, cerebrospinal fluid leak, or requiring placement of a drain

Design outcomes

Primary

MeasureTime frame
Assessment of postoperative analgesia in term of VAS score after epidural application of gel foam soaked in morphine ropivacaine morphine ropivacaine combination in patients undergoing single level lumbar laminectomyTimepoint: 24 HOURS

Secondary

MeasureTime frame
1 Duration of analgesia 2 Total 24 hour rescue analgesic consumption 3 RAMSAY SEDATION SCORE 4 Patient satisfaction Timepoint: 24 hours

Countries

India

Contacts

Public ContactDr Geeta Singariya

Dr S N medical collage, Jodhpur

drlovieanaesthesia@gmail.com8360114502

Outcome results

None listed

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