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N/A Completed N=90

Remifentanil Versus Dexmedetomidine for Post-Cardiac Surgery Patients With Noninvasive Ventilation Intolerance

Source: ClinicalTrials.gov NCT03395886 ↗
Enrolled (actual)
90
Serious AEs
0.0%
Results posted
Nov 2019
Primary outcomePrimary: Number of Participants With NIV Failure — 10; 8 Participants — p=0.831

Summary

The aim of this study is to compare the sedation effects between remifentanil and dexmedetomidine in post-cardiac surgical patients who developed noninvasive ventilation (NIV) intolerance.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With NIV Failure
10; 8 0.831
SECONDARY
Number of Participants With NIV Mitigation
44; 31 0.800

Eligibility Criteria

Inclusion Criteria

  • adult patients
  • after cardiac surgery
  • receiving noninvasive ventilation
  • moderate to severe NIV intolerance (NIV intolerance score of 3 or 4)

Exclusion Criteria

  • difficult expectoration
  • pregnancy or breastfeeding
  • intensive care delirium screening checklist score more than 4
  • drug abuse history
  • known allergy to opiods
  • cardiogenic shock
  • malignant arrhythmias
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03395886). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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