Health Condition 1: M489- Spondylopathy, unspecified
Conditions
Interventions
Intervention1: Erector Spinae Plane Block: After giving General anesthesia by Institute protocol patient put on prone position following which under sterile precautions linear ultrasound probe (8-13hz
Sponsors
Jawaharlal Institute of Postgraduate Medical Education and Research
Eligibility
Inclusion criteria
Inclusion criteria: ASA 1 & 2 Type of surgery(elective lumbosacral spine surgery)
Exclusion criteria
Exclusion criteria: patient refusal patient with history of allergy to local anesthetics patient with coagulopathies or on anticoagulants infection at injection site
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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.Timepoint: 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
| Measure | Time frame |
|---|---|
| To Compare Hemodynamic Parameters and Surgical Pleth Index Numeric rating pain scale surgical stress response by measuring serum cortisol IL 6 and IL 10 Intraoperative requirement of fentanyl Timepoint: Hemodynamic Parameters like Heart Rate Mean Arterial Pressure Spo2 Surgical Pleth Index will be measured every 10 minutes from the Time before Induction to the End of Surgery Total Intraoperative Fentanyl Reuirement will be noted serum cortisol and interleukins IL6 and IL10 measured pre induction at the most traumatic point of surgery and 24 hours postoperative period respectively | — |
Countries
India
Contacts
Public ContactDr S Adinarayanan
Jawaharlal Institute of Postgraduate Medical Education and Research
Outcome results
None listed