Perineural additives in ultrasound guided supraclavicular brachial plexus block
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Patients undergoing upper limb orthopaedic procedures
- Registration Number
- CTRI/2018/08/015438
- Lead Sponsor
- BGS GLOBAL HOSPITALS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
Patients undergoing unilateral upper limb surgeries of ASAI-II PS
Exclusion Criteria
Patient refusal Weight ,50 kg Infection at site of block Known hypersensitivity to drug Pregnants and lactating women
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of postoperative analgesiaTimepoint: In the postoperative period patients were assessed for pain and request for analgesic at 30 minute intervals till 360 minutes from the time of completion of injection. Thereafter hourly till 720 minutes and then at 900 minutes and 1440 minutes until administration of rescue analgesic
- Secondary Outcome Measures
Name Time Method Duration of motor blockTimepoint: In the postoperative period patients were assessed for motor power at 30 minute intervals till 360 minutes from the time of completion of injection. Thereafter hourly till 720 minutes and then at 900 minutes and 1440 minutes until recovery of full motor power;Duration of sensory blockTimepoint: In the postoperative period patients were assessed for sensation at 30 minute intervals till 360 minutes from the time of completion of injection. Thereafter hourly till 720 minutes and then at 900 minutes and 1440 minutes until resolution of block;SedationTimepoint: In the postoperative period patients were assessed for sedation at 30 minute intervals till 360 minutes from the time of completion of injection. Thereafter hourly till 720 minutes and then at 900 minutes and 1440 minutes until administration of rescue analgesic