Status:

TERMINATED

The Effects of Dexmedetomidine and Remifentanil on Carotid Patients

Lead Sponsor:

The Cleveland Clinic

Conditions:

Carotid Artery Stenosis

Eligibility:

All Genders

50-80 years

Phase:

PHASE4

Brief Summary

We propose to test whether intraoperative administration of dexmedetomidine will reduce hemodynamic control in the intra- and post-operative periods and reduces PACU analgesic requirements in patients...

Detailed Description

Remifentanil is an amidopiperidine derivative with unique pharmacokinetic properties. Its steady-state volume of distribution is 30 L (3). Its context-sensitive half life is consistently short (3.2 mi...

Eligibility Criteria

Inclusion

  • Consenting adult patients (age \>50 years) undergoing carotid endarterectomy with general anesthesia.

Exclusion

  • Receiving another alpha 2-adrenoreceptor agonist;
  • Contraindication to dexmedetomidine, including allergy;
  • Current hepatic disease (liver function tests \> twice upper limit of normal);
  • Renal insufficiency, as defined by a creatinine \> 2.0 mg/dL;
  • Mentally impairment, including dementia or delirium;
  • Heart block ;
  • Sick sinus syndrome;
  • Atrial fibrillation with a low ventricular response (\< 50 bpm);
  • Absolute or relative hypovolemia;
  • Prior stroke;
  • Severe left-ventricular dysfunction

Key Trial Info

Start Date :

June 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2008

Estimated Enrollment :

142 Patients enrolled

Trial Details

Trial ID

NCT00335972

Start Date

June 1 2006

End Date

May 1 2008

Last Update

August 11 2017

Active Locations (1)

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1

Cleveland Clinic

Cleveland, Ohio, United States, 44195

The Effects of Dexmedetomidine and Remifentanil on Carotid Patients | DecenTrialz