Post operative pain relief in lumber spine surgery patients

Phase 4

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

• Registration Number: CTRI/2023/07/055003
• Lead Sponsor: M D M Hospital Dr S N Medical College Jodhpur

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 25 July 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

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

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
1 Duration of analgesia <br/ ><br>2 Total 24 hour rescue analgesic consumption <br/ ><br>3 RAMSAY SEDATION SCORE <br/ ><br>4 Patient satisfaction <br/ ><br>Timepoint: 24 hours