Trials / Completed
CompletedNCT01975285
Efficacy of Popliteal Nerve Blocks With and Without Dexamethasone on the Duration of Analgesia for Foot & Ankle Surgery
Prospective Randomized Double Blind Study to Evaluate the Efficacy of Popliteal Nerve Blocks With and Without Dexamethasone on the Duration of Analgesia for Foot & Ankle Surgery.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Cedars-Sinai Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this research study to evaluate the effects of dexamethasone as an addition to peripheral nerve block (Put the nerve to sleep with Bupivacaine a numbing medication) on length of pain relief (analgesia), postoperative narcotic (opioids) requirements, pain scores, and patient satisfaction after foot and ankle procedures.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dexamethasone | 0.5% Bupivacaine with 1:200,000 epinephrine + Dexamethasone 4mg per 20cc |
| DRUG | Saline | 0.5% Bupivacaine with 1:200,000epinephrine + Saline 1 ml per 20cc |
Timeline
- Start date
- 2013-08-01
- Primary completion
- 2014-06-01
- Completion
- 2014-06-01
- First posted
- 2013-11-04
- Last updated
- 2016-05-06
- Results posted
- 2016-05-06
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01975285. Inclusion in this directory is not an endorsement.