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
| Type | Name | Description |
|---|---|---|
| DRUG | Ropivacaine 0.5% Injectable Solution | 30 mL Ropivacaine 5 mg/mL (= 150 mg Ropivacaine) |
| DRUG | Lidocaine epinephrine | 20 mL Ropivacaine 5 mg/mL + 10 mL Lidocaine-Epinephrine (20 mg + 5 μg) / ml (= 100 mg Ropivacaine + 200 mg Lidocaine) |
| DRUG | Ropivacaine 0.75% Injectable Solution | 20 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.