Trials / Completed
CompletedNCT03065309
Determination of Remifentanil's ED50 for Rapid Sequence Intubation Avoiding Bradycardia and Hypotension in Adults
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 15 (actual)
- Sponsor
- Brasilia University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This study will find the median effective dose of remifentanil for rapid sequence intubation which avoids bradycardia and hypotension
Detailed description
Remifentanil is becoming popular for rapid sequence intubation because it has a fast onset and ultra-short half-life. Remifentanil a potent opioid associated to bradycardia and hypotension at high doses.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Remifentanil | bolus dose |
Timeline
- Start date
- 2017-02-25
- Primary completion
- 2017-02-28
- Completion
- 2017-03-01
- First posted
- 2017-02-27
- Last updated
- 2017-09-13
Locations
1 site across 1 country: Brazil
Source: ClinicalTrials.gov record NCT03065309. Inclusion in this directory is not an endorsement.