Clinical Trials Directory

Trials / Completed

CompletedNCT06381622

Combining Lidocaine and Ropivacaine for an Infraclavicular Brachial Plexus Nerve Block

The Effect of Combining Lidocaine and Ropivacaine on the Duration and Onset Time of an Ultrasound-guided Infraclavicular Brachial Plexus Nerve Block. a Randomized Controlled Trial

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
78 (actual)
Sponsor
Nordsjaellands Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is to investigate how the combination of ropivacaine (a slow onset, long duration local anesthetic) with lidocaine (a rapid onset, shorter duration local anesthetic) affects the onset and duration of a lateral infraclavicular plexus brachialis (LIC) block in patients undergoing non-acute hand surgery.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine 0.5% Injectable Solution30 mL Ropivacaine 5 mg/mL (= 150 mg Ropivacaine)
DRUGLidocaine epinephrine20 mL Ropivacaine 5 mg/mL + 10 mL Lidocaine-Epinephrine (20 mg + 5 μg) / ml (= 100 mg Ropivacaine + 200 mg Lidocaine)
DRUGRopivacaine 0.75% Injectable Solution20 mL Ropivacaine 7,5 mg/mL + 10 mL Lidocaine-Epinephrine (20 mg + 5 μg)/mL (= 150 mg Ropivacaine + 200 mg Lidocaine)

Timeline

Start date
2024-04-18
Primary completion
2024-10-24
Completion
2024-11-23
First posted
2024-04-24
Last updated
2025-02-17

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT06381622. Inclusion in this directory is not an endorsement.