TerminatedPhase 3ACTRN12605000231640

A clinical trial of dexmedetomidine or remifentanil sedation for awake fibreoptic intubation


Sponsor

Dr Sarah Harper

Enrollment

20 participants

Start Date

Nov 30, 2004

Study Type

Interventional

Conditions


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a clinical trial of dexmedetomidine or remifentanil sedation for awake fibreoptic intubation. You may be eligible if you are adults aged 18 and older who awake fibreoptic intubation, no contraindication to remifentanil or dexmedetomidine. People with chronic alpha-2 agonist or opioid therapy, allergy or previous adverse reaction to study drugs, uncontrolled hypertension may not be able to participate. Participation may involve medical tests, study visits, and follow-up appointments.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Dexmedetomidine 0.7 mcg/kg then 0.4 mcg/kg/h until completion of procedure

Dexmedetomidine 0.7 mcg/kg then 0.4 mcg/kg/h until completion of procedure


Locations(1)

Australia

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ACTRN12605000231640


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