Comparision of analgesic efficacy between USG guided Erector Spinae Plane Block and Quadratus Lumborum Block in adult elective abdominal hysterectomy surgeries under Spinal Anaesthesia
Overview
- Phase
- Phase 2/3
- Status
- Not yet recruiting
- Sponsor
- AIIMS Raebareli
- Enrollment
- 40
- Locations
- 1
- Primary Endpoint
- 1.To compare the duration of analgesia between Erector Spinae Plane Block and Quadratus Lumborum block .
Overview
Brief Summary
This is a Randomized, double blinded study comparing the analgesic efficacy of USG guided Erector Spinae Plane block and Quadratus Lumborum block in adult elective abdominal hysterectomy surgeries under spinal anaesthesia is being conducted in AIIMS , Raebareli. The primary outcome is to compare the duration of analgesia between Erector Spinae Plane Block and Quadratus Lumborum Block and to compare the total dose of tramadol consumed as rescue analgesia in post operative 48 hours in both groups.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •BMI between 24-30 kg/m2
- •height between 150-170 cm
- •Duration of Surgery-1.5 to 2 hours
- •Patients of ASA 1 and 2
- •patients undergoing Total Abdominal Hysterectomy.
Exclusion Criteria
- •1.Patient refusal for procedure 2.Patients having Coagulopathy 3.Patients having cerebrovascular disease 4.Patients having systemic infection 5.Inability to understand the study protocol 6.Patients who have Allergy to local anesthetics 7.Psychopathy that may affect patient evaluation 8.Pregnant Patients 9.Infection at site of injection 10.Patients with Liver disease 11.Patients with kidney disease.
Outcomes
Primary Outcomes
1.To compare the duration of analgesia between Erector Spinae Plane Block and Quadratus Lumborum block .
Time Frame: 48 hours
2.To compare the total dose of tramadol needed as rescue analgesia in post operative 48 hours in both groups.
Time Frame: 48 hours
Secondary Outcomes
- 1.To compare the hemodynamic parameters between the groups.
Investigators
Dr Pallav Pattnaik
All India Institute Of Medical Sciences, Raebareli