A study to compare the effects of Bupivacaine withLignocaine and Ropivacaine with Lignocaine in Brachial Plexus Block.
Not Applicable
- Conditions
- Health Condition 1: 4- Measurement and Monitoring
- Registration Number
- CTRI/2021/08/035536
- Lead Sponsor
- Shyamaldip Gurung
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Grade 1 & 2 undergoing surgery of upper limb.
Exclusion Criteria
1.Patients refusal/ Uncooperative patients
2.Patients having diabetes, hypertension,
neuropathy, peripheral nerve injury.
3.Pregnant and lactating patients.
4.Patients on anticoagulants or bleeding disorders.
5.Patients with history of hypersensitivity to amide group of local anaesthetic agents.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset time of sensory and motor block. <br/ ><br>Timepoint: Assessment at 5 minutes, 10 minutes, 15 minutes and 20 minutes. <br/ ><br>
- Secondary Outcome Measures
Name Time Method Duration of postoperative analgesia <br/ ><br>Timepoint: Assessment at 2 hours, 4 hours and 6 hours.