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pain relief need in arm surgeries after giving interscalene and erector spinae plane block

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/03/050905
Lead Sponsor
Hamdard institute of medical sciences and research and Hakeem Abdul Hameed hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

All patients aged 18-65 years posted for unilateral proximal humerus surgeries with American society of anaesthesiologist physical status one and two shall be included in the study

Exclusion Criteria

1.Patient refusal

2.Patient with known allergy to local anaesthetics

3.Patients with coagulopathies

4.Patients with infection at injection sites

5.Patients with prior opioid addiction or analgesic abuse

6.Patients with BMI less than 18.5 kg/m2 and greater than 34.9 kg/m2

7.Patients with prior cervical or thoracic spine surgery

8.Patients with liver or renal insufficiency

9.Patients with mental illness

10.Patients with pre existing neuropathy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the efficacy of ultrasound guided erector spinae plane block at T2 versus interscalene brachial plexus block using 20 ml of 0.125% bupivacaine for post operative analgesia in patients undergoing proximal and mid humerus surgeries.Timepoint: To compare the efficacy of ultrasound guided erector spinae plane block at T2 versus interscalene brachial plexus block using 20 ml of 0.125% bupivacaine for post operative analgesia immediate post op, 1hr,2hr,6hr,12hr,24hr
Secondary Outcome Measures
NameTimeMethod
1.To compare postoperative motor function in the two groups <br/ ><br> <br/ ><br>2.To compare total intraoperative fentanyl requirement in the two groups <br/ ><br> <br/ ><br>3.To compare the requirement of first rescue analgesic in terms of hours after surgery in the two groups <br/ ><br>4.To compare patient satisfaction scores in the two groups <br/ ><br>Timepoint: postoperative motor function immediate post op, intraoperative fentanyl requirement , requirement of first rescue analgesic , patient satisfaction score after 24 hrs
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