Techniques of providing pain relief during placement of cannula in the neck
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/04/051345
- Lead Sponsor
- Department of Anaesthesia and Intensive Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
trauma patients scheduled for awake ultrasound-guided central line placement in the internal jugular vein will be included in the study
Exclusion Criteria
patients with coagulopathy, infection at the insertion site, patients with psychiatric illness, patients with focal neurological deficits, patients with allergy to any of the drugs used in the study and patients who refuse consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain during central line insertionTimepoint: At baseline
- Secondary Outcome Measures
Name Time Method 1. Central line insertion time (time interval from needle insertion to end of suturing) <br/ ><br>2. Patient discomfort during the procedure as measured by 11-point verbal numeric rating discomfort scale (VNRDS) from 0 to 10 (0: None, 10: Extreme discomfort)5 <br/ ><br>3. Complications, if any <br/ ><br>Timepoint: At the time of central line insertion