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)
View Full Details on ANZCTR
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ACTRN12605000231640
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