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The Comparison Of Two Fascial Plane Blocks For Post Operative Analgesia In Abdominal Surgeries.

Not Applicable
Conditions
Health Condition 1: K638- Other specified diseases of intestine
Registration Number
CTRI/2022/02/040346
Lead Sponsor
Himalayan Institute Of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)Age - 18-65 Years

2)Genderâ?? Both male and female patient

3)Physical Status :American Society of Anesthesiologists (ASA) I and II patients

scheduled to undergo upper abdominal surgeries with midline incision

Exclusion Criteria

1)American Society of Anaesthesiologists(ASA) physical status more than or equal to III patients

2)Local infection at the site of block

3)H/o allergy to study medications

4)Patients on chronic pain relief medications

5)Allergic to local anesthetics

6)Bleeding disorders

7)Dyselectrolytemias

8)Patient on anti-coagulants

9)Inability to give informed consent

10)Severe cardiovascular , respiratory, liver and kidney disease

11)Patient who cannot operate Patient Controlled Analgesia (PCA) system

12)Psychiatric disorders

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To observe and evaluate post operative analgesic efficacy of ultrasound guided Bilateral Quadratus Lumborum block and Bilateral Erector Spinae block in abdominal surgeries with midline incision.Timepoint: To observe the total post operative fentanyl consumption over 24 hrs after administration of each block in either group and to study pain intensity at 0,4,8,12,16,20 and 24 hrs intervals respectively.
Secondary Outcome Measures
NameTimeMethod
The secondary outcome variable will be Motor block.It will be evaluated using modified Bromage Score.Timepoint: It will be calculated at time points 0,4,8,12,16,20 and 24â??h after anesthesia recovery.
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