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Comparing the two drugs Ropivacaine Vs Bupivacaine in Quadratus Lumborum block using sonography for post surgical pain relief in Laparascopic Appendectomy surgeries.

Not Applicable
Conditions
Health Condition 1: K36- Other appendicitis
Registration Number
CTRI/2022/02/040630
Lead Sponsor
GMERS Medical college and Hospital Gotri
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1)AGE: 18-55years

2)BMI: 19-25kg/m2

3)American society of anaesthesia physical status 1 & 2

4)patients giving consent for the procedure

Exclusion Criteria

1)History of allergy to study drugs

2)Infection at local site

3)Altered coagulation profile

4)Patients on chronic pain medications

5)History of known lower limb muscle weakness

6)Known systemic disease concerning CVS, RS, CNS, psychiatric, Renal, Liver, musculoskeletal systems

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The time to the requirement of first rescue analgesia observed in both the study groups subjected to either Injection Ropivacaine 0.375% or Bupivacaine 0.25% for postoperative analgesia in USG guided bilateral Quadratus lumborum blockTimepoint: the patients will be assessed for post operative analgesia after the giving of block immediately till VAS of more than four was observed and this duration will be considered as total duration of analgesia
Secondary Outcome Measures
NameTimeMethod
1)Total consumption of analgesics in the postoperative period <br/ ><br>2)Stability of patients vital parameters <br/ ><br>3)Patient satisfaction score-poor, fair, good, excellent <br/ ><br>4)Complications related to procedure if anyTimepoint: total consumption of analgesia after rescue analgesia till 30 hours postoperatively <br/ ><br>vital parameters to be observed in the post operative period 30 min, 60 min, 90 min 2,4,6,12,18,24, till 30 hours <br/ ><br>patient satisfaction score as fair, good excellent till 30 min post block once the onset starts <br/ ><br>complications related to procedure immediate and till 30 hours of the study time
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