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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03065309
Other study ID # TCC-Lara-2017
Secondary ID
Status Completed
Phase Phase 3
First received February 22, 2017
Last updated September 12, 2017
Start date February 25, 2017
Est. completion date March 1, 2017

Study information

Verified date September 2017
Source Brasilia University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will find the median effective dose of remifentanil for rapid sequence intubation which avoids bradycardia and hypotension


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.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date March 1, 2017
Est. primary completion date February 28, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Indication of anesthesia induction

Exclusion Criteria:

- Protocol violation

- Monitoring problems

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Remifentanil
bolus dose

Locations

Country Name City State
Brazil Hospital das Forças Armadas Brasilia Distrito Federal

Sponsors (1)

Lead Sponsor Collaborator
Brasilia University Hospital

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary hemodynamic stability during rapid sequence intubation no bradycardia and no hypotension from anesthesia induction up to 5 minutes
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