Trials / Completed
CompletedNCT01690663
Dose Response Study of Dexamethasone in Combination With Bupivacaine 0.25%
Dose Response Study of Dexamethasone in Combination With Bupivacaine 0.25% in Ultrasound Guided Supraclavicular Brachial Plexus Nerve Block, a Randomized, Placebo Controlled Prospective Clinical Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 89 (actual)
- Sponsor
- University of Pennsylvania · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
When used in conjunction with a local anesthetic, dexamethasone may prolong both the sensory and motor effects of high supraclavicular brachial plexus nerve block (SBP) in arthroscopic shoulder surgery. This study seeks to determine if there is a relationship between the duration of sensory and motor blockade in supraclavicular brachial plexus nerve blocks (SBP) when combined with increasing doses of dexamethasone.
Detailed description
The exact mechanism of dexamethasone on peripheral nerve block is unclear. The current theory is that the effect is not dose related, while only 4mg and 8mg doses were studied. Our hypothesis is that the dose differences at 1mg, 2mg, or 4mg, does not have significant effect on the duration of analgesia. Therefore, we are not considering any patients to receive suboptimal dosing of preservative free dexamethasone in this study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine 0.25% | |
| DRUG | Dexamethasone | |
| DRUG | normal saline | placebo |
Timeline
- Start date
- 2012-09-01
- Primary completion
- 2015-02-01
- Completion
- 2015-02-01
- First posted
- 2012-09-24
- Last updated
- 2017-05-04
- Results posted
- 2017-05-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01690663. Inclusion in this directory is not an endorsement.