A clinical trial to compare the efficacy of two different anaesthetic agents in upper limb surgeries
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/065128
- Lead Sponsor
- Smitakshi Das
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA grade 1 and 2
2.Patient posted for elective orthopaedic elbow, forearm and hand surgeries under USG guided supraclavicular brachial plexus block
3.Patients giving consent to participate in the study
Exclusion Criteria
1.Coagulation disorders and patient on anticoagulants
2.Infection at site of injection
3.History of anaphylaxis to local anaesthetics and allergy to the study drugs
4.Patients with peripheral neuropathy.
5.Patients on chronic analgesic medications
6.Patients with contralateral phrenic nerve palsy.
7.Block failure or partial blocks
8.Pregnant and lactating patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of sensory block in each groupTimepoint: 24hrs
- Secondary Outcome Measures
Name Time Method Duration of analgesiaTimepoint: 24 hours;Duration of motor blockTimepoint: till full recovery of motor function;Hemodynamic changes following blockTimepoint: During intraoperative period;Onset of sensory block and motor blockTimepoint: 30mins;Side effects and complicationsTimepoint: 24 hours