Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Superficial cervical plexus block: The superficial cervical plexus block will be administered at the time of central line insertion
Control Intervention1: Local anesthetic infiltration:
Sponsors
Department of Anaesthesia and Intensive Care
Eligibility
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain during central line insertionTimepoint: At baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Central line insertion time (time interval from needle insertion to end of suturing) 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 3. Complications, if any Timepoint: At the time of central line insertion | — |
Countries
India
Contacts
Public ContactNidhi Bhatia
PGIMER
Outcome results
None listed