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Comparison of postoperative pain relief by two types of nerve blocks after arthroscopic knee surgery.

Phase 3
Conditions
Health Condition 1: S833- Tear of articular cartilage of knee, current
Registration Number
CTRI/2023/11/059394
Lead Sponsor
Government medical college and hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1 Age between 18 to 65 years

2 American society of anaesthesiologists (ASA) physical status 1 and 2

3.BMI 18 to 30 kg/m2

4 patients scheduled for knee arthroscopy

Exclusion Criteria

1 patients refusing to give informed consent

2 patients with history of relevant drug allergy

3 patients with history of psychiatric illness and substance abuse

4 patients with severe cardiovascular respiratory metabolic or neurological disorders

5 pregnant and lactating women

6 patients with coagulopathy and bleeding disorders

7 infection at planned injection site

8 patient on steroids

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
rescue fentanyl consumptionTimepoint: 4 hour, 12 hour, 24 hour
Secondary Outcome Measures
NameTimeMethod
Pain scores on NRSTimepoint: 4 12 and 24 hours after administration of block;Patient satisfaction on 0- 100 VASTimepoint: 4 12 24 hours after administration of block;Sensory and motor blockadeTimepoint: 4 12 24 hours after administration of block;Side effectsTimepoint: 4 12 24 hours after administration of block;Time to first rescue analgesia <br/ ><br>Timepoint: Immediately after the block then 5 10 15 60 minutes followed by 4 12 24 hour interval
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