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Clinical Trials/CTRI/2021/11/038112
CTRI/2021/11/038112
Not yet recruiting
未知

Comparison of dose of Propofol when used in combination with ketamine versus Fentanyl for sedation and anti inflammatory effects in mechanically ventilated patients A double blind randomised controlled study

AIIMS Jodhpur0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: J952- Acute pulmonary insufficiency following nonthoracic surgeryHealth Condition 2: B968- Other specified bacterial agents as the cause of diseases classified elsewhereHealth Condition 3: I999- Unspecified disorder of circulatory system
Sponsor
AIIMS Jodhpur
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • All ICU patients between 18 to 80 years who are expected to be on mechanical ventilation for more than 48 hours

Exclusion Criteria

  • 1\) Patients weaned of mechanical ventilation within 48 hrs of mechanical ventilation
  • 2\) Patients who are on non invasive mode of ventilation
  • 3\) Patients who had cardiac arrest and received CPR within 48 hrs of mechanical ventilation
  • 4\) Patients having history of dementia, Psychiatric disorder, on antipsychotic or antidepressants prior to ICU admission
  • 5\) Pregnant females and patients having known hypersensitivity to any of the sedative agents
  • 6\) Cardiogenic shock, Acute decompensated heart failure, MI
  • 7\) Patients having end stage liver failure ( Child Pugh C)
  • 8\) Primary neurological injury (TBI, Stroke, SCI, Anoxic brain injury, Brain edema)
  • 9\) Hemodynamically unstable patients

Outcomes

Primary Outcomes

Not specified

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