In lower spine surgery-comparing the pain relief duration with erector spinae plane block and single shot epidural techniques

Not yet recruiting

• Conditions: Spondylopathy, unspecified,

• Registration Number: CTRI/2019/06/019630
• Lead Sponsor: Jawaharlal Institute of Postgraduate Medical Education and Research

Brief Summary

This study involves two groups  group 1  patients undergoing elective lumbosacral spine surgery will be given erector spinae plane block after receiving general anesthesia in prone position by ultrasound guidance, other group will receive single shot epidural analgesia by loss of resistance technique in awake state in left lateral position after which general anesthesia will be given under institute protocol. We are comparing the analgesic efficacy by noting and comparing duration of analgesia and the time at which patient asks for rescue analgesia and by assessing pain score using numeric rating score in the postoperative period upto 48 hours.

Detailed Description

Not available

Study Timeline

• Study Start: 2019-01-07
• Last Update Posted: 2019-10-06

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 74

Inclusion Criteria

ASA 1 & 2 Type of surgery(elective lumbosacral spine surgery).

Exclusion Criteria

patient refusal patient with history of allergy to local anesthetics patient with coagulopathies or on anticoagulants infection at injection site.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparison of Analgesic Efficacy of the Erector Spinae Block with Single Shot Epidural Analgesia in Patients Undergoing Lumbosacral Spine Surgery by Comparing the Duration of Analgesia between both groups.	Time at which the patient asks for Rescue Analgesia for the first time within 48 hours by assessing the | Numeric Rating Pain Scale NRS 1 to 3 is Mild NRS 4 to 7 is Moderate and NRS more than 7 is Severe pain respectively which is recorded at 4 8 12 16 20 24 and 48 hours respectively in Postoperative Period

Secondary Outcome Measures

Name	Time	Method
To Compare	Hemodynamic Parameters and Surgical Pleth Index

Trial Locations

Locations (1)

Jawaharlal Institute of Postgraduate Medical Education and Research; 🇮🇳 Pondicherry, PONDICHERRY, India

Jawaharlal Institute of Postgraduate Medical Education and Research

🇮🇳Pondicherry, PONDICHERRY, India

Dr Ramya

Principal investigator

9531833300

dr.ramya.suneel@gmail.com