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Cerebral Vascular Effects of Dexmedetomidine Versus Propofol Sedation in Intubated Mechanically Ventilated ICU Patients (DEXSEDATION)

A

Assiut University

Status and phase

Suspended
Phase 3
Phase 2

Conditions

Sedation

Treatments

Drug: 10-70 mcg/kg/h propofol infusion.
Drug: 0.2-0.7 mcg/kg/h dexmedetomedine infusion.

Study type

Interventional

Funder types

Other

Identifiers

NCT03285165
17200002

Details and patient eligibility

About

Serial transcranial Doppler (TCD) exams in healthy volunteers and in animal models showed a strong linear relationship between middle cerebral artery (MCA) flow velocity (FV) and dexmedetomidine infusion. The concomitant elevation of pulsatility index (PI) indicates vasoconstriction of the cerebral vasculature as the most profound underlying mechanism.

Full description

Available clinical evidence on the use of dexmedetomidine sedation in neurosurgical and neurocritical care is limited and no definite conclusion can be drawn. There is a need for The use of dexmedetomidine might be a useful adjunct in clinical situations when the increase in CBF could be detrimental such as vasogenic cerebral edema (i.e., TBI, large brain tumors). However, dexmedetomidine sedation is questionable in patients with subarachnoid hemorrhage and acute stroke, since the associate drop in arterial pressure could worsen the coexisting increase in circulating catecholamines and massive sympathetic outflow. Further high-quality RCTs to evaluate the use of dexmedetomidine as a sedative agent both in general ICU patients and in patients with TBI.

Transcranial Doppler (TCD) is a simple noninvasive bedside tool to assess the cerebral blood flow pattern. The new development of transcranial color Doppler with angle correction option helps to improve the sensitivity of test results. TCD can assess the evolution of CBF alterations and possibly cerebral autoregulation performance and ICP estimation in patients presenting with cerebral pathology.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult trauma patients (18-50 years old, ASA I-II).
  • With and without mild TBI.
  • Mild traumatic brain injury will include; brain edema, brain contusion, fracture base, fissure fracture and depressed fracture.
  • The severity of traumatic brain injury will be defined as mild based on basal Glasgow Coma Scale and basal Computerized tomography scanning.
  • Requirements of endotracheal intubation, mechanical ventilation and light to moderate sedation because of associated abdominal or chest traumatic injuries.
  • The sedation needed should of an estimated duration not less than 24h.
  • Baseline hemodynamic parameters within the normal range.
  • Baseline middle cerebral artery flow velocity within the normal range.

Exclusion criteria

  • Severe traumatic brain injury, subarachnoid hemorrhage and Intra-cerebral hemorrhage.
  • Spinal cord injury.
  • Hemodynamically unstable patients and patients on inotropes.
  • Patients who have a cardiac pacemaker or automatic implantable cardioverter defibrillator.
  • Patients with hepatic or renal impairment.
  • Pregnant females.
  • Patients who are incarcerated.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 4 patient groups

DEX I
Active Comparator group
Description:
Trauma Patients without TBI received 0.2-0.7 mcg/kg/h dexmedetomedine infusion.
Treatment:
Drug: 0.2-0.7 mcg/kg/h dexmedetomedine infusion.
DEX II
Active Comparator group
Description:
Trauma Patients with TBI received 0.2-0.7 mcg/kg/h dexmedetomedine infusion.
Treatment:
Drug: 0.2-0.7 mcg/kg/h dexmedetomedine infusion.
Propofol I
Active Comparator group
Description:
Trauma Patients without TBI received 10-70 mcg/kg/h propofol infusion.
Treatment:
Drug: 10-70 mcg/kg/h propofol infusion.
Propofol II
Active Comparator group
Description:
Trauma Patients with TBI received 10-70 mcg/kg/h propofol infusion.
Treatment:
Drug: 10-70 mcg/kg/h propofol infusion.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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