Trials / Completed
CompletedNCT03649763
Onset and Duration of Forearm Nerve Blockade
Onset and Duration of Forearm Nerve Blockade Performed With a Single Distal Injection Versus Sequential Injections at Distal and Proximal Locations Alongside the Nerves: A Blinded Randomized
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 36 (actual)
- Sponsor
- New York School of Regional Anesthesia · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Accepted
Summary
This pilot study will evaluate the latency of onset and duration of sensory-motor block in patients undergoing hand surgery. Patients will be randomized to receive nerve blocks of the distal forearm or of the distal and proximal forearm. Local anesthetic will be injected to anesthetise the median and ulnar nerves in the distal forearm (1-injection site group) or the median and ulnar nerves in the distal and proximal forearm (2-sequential injection sites group) to accomplish anesthesia for surgery on the hand.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine | lidocaine 1%, distal ( ulnar and medial nerve): 6ml/nerve , 12m total |
| DRUG | Bupivacaine | Bupivacaine 0.5%,distal ( ulnar and medial nerve): 6ml/nerve , 12m total |
| DRUG | Lidocaine | lidocaine 1%, distal and proximal ( ulnar and medial nerve): 3ml/nerve , 12m total |
Timeline
- Start date
- 2018-03-07
- Primary completion
- 2018-12-31
- Completion
- 2018-12-31
- First posted
- 2018-08-28
- Last updated
- 2019-02-26
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT03649763. Inclusion in this directory is not an endorsement.