Trials / Completed
CompletedNCT02454868
Remifentanil Minimum Effective Dose for Children Intubation Without Neuromuscular Blockade
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Brasilia University Hospital · Academic / Other
- Sex
- All
- Age
- 2 Years – 9 Years
- Healthy volunteers
- Accepted
Summary
Introduction: remifentanil's optimal dose for children intubation without neuromuscular blockade is unknown. Method: phase IV adaptative trial using Dixon's up-and-down method for modeling remifentanil's dose-response curve for adequate intubation conditions as defined by previous studies.
Detailed description
Introduction: remifentanil's optimal dose for children intubation without neuromuscular blockade is unknown. Method: phase IV adaptative trial using Dixon's up-and-down method for modeling remifentanil's dose-response curve for adequate intubation conditions as defined by previous studies. Remifentanil doses starting from 2mg/kg will be infused before intubation. When a success occurs next patient's dose will be decreased by 0.25mg/kg/h. When a success does not occur the next patient's dose will be increased by 0.25mg/kg/h. Intubation will be considered adequate if patient does not cough, does not move, if vocal cords are open, if larigocsocpic Cormack grade I or II.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Remifentanil | Remifentanil for intubation without neuromuscular blockade |
Timeline
- Start date
- 2016-07-01
- Primary completion
- 2016-07-01
- Completion
- 2016-07-01
- First posted
- 2015-05-27
- Last updated
- 2016-07-19
Source: ClinicalTrials.gov record NCT02454868. Inclusion in this directory is not an endorsement.