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Determination of Remifentanil's ED50 for Rapid Sequence Intubation Avoiding Bradycardia and Hypotension in Adults

B

Brasilia University Hospital

Status and phase

Completed
Phase 3

Conditions

Hypotension
Bradycardia

Treatments

Drug: Remifentanil

Study type

Interventional

Funder types

Other

Identifiers

NCT03065309
TCC-Lara-2017

Details and patient eligibility

About

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

Full 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.

Enrollment

15 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Indication of anesthesia induction

Exclusion criteria

  • Protocol violation
  • Monitoring problems

Trial design

15 participants in 1 patient group

Single Arm
Experimental group
Description:
Patients will receive bolus dose of remifentanil before intubation
Treatment:
Drug: Remifentanil

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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