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Clinical Trials/NCT00991328
NCT00991328TerminatedPhase 3

Tailored Patient Management Guided With Absolute Cerebral Oximetry to Prevent Neurocognitive Injury in Elderly Patients Undergoing Cardiac Surgery.

Icahn School of Medicine at Mount Sinai1 site in 1 country15 target enrollmentStarted: September 1, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 3
Status
Terminated
Enrollment
15
Locations
1
Primary Endpoint
The association of Postoperative Delirium (PD) and Postoperative Cognitive Dysfunction (POCD) with changes in cerebral tissue oxygen saturation (SctO2).

Study Overview

Brief Summary

The purpose of this study is to determine whether brain oxygenation measured by cerebral oximeter has an impact on neurocognitive dysfunction.

Detailed Description

Both postoperative delirium (PD) and postoperative cognitive dysfunction (POCD) are well known complications seen in elderly patients after cardiac surgery. The etiologies of PD and POCD are unknown, but cerebral ischemia remains a prime candidate. Attempts to correlate reduced levels of systemic oxygenation (i.e. SpO2) with the development of PD/POCD have been to date disappointing.

We believe that cerebral oximetry, a noninvasive technology that continuously monitors cerebral tissue oxygen saturation (SctO2), will enable us to answer the question of whether or not a correlation exists.

The availability of an absolute cerebral oximeter (FORE-SIGHT), with its ability to establish and manipulate threshold values for SctO2, provides us the opportunity to assess the relationship between cerebral oxygenation and the development of neurocognitive complications.

We propose a randomized, masked trial of 120 patients, adequately powered to assess the following:

  • Is there an association between deficits in cerebral oxygenation and the occurrence of PD at some time in the 1st 5 days after the operation?
  • Is there an association between deficits in cerebral oxygenation and changes in POCD scores shortly (5 days) after the operation and/or 4-6 weeks later? We hypothesize that individually tailored patient management guided with intraoperative and postoperative absolute cerebral oximetry monitoring using a tailored protocol designed to maintain SctO2 values above a specific threshold will result in improved neurocognitive outcomes in geriatric patients undergoing cardiac surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Care Provider, Investigator)

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •65 and older
  • •Elective cardiac or thoracic aortic surgery
  • •Capable and willing to consent
  • •Participants literate in English

Exclusion Criteria

  • •Emergency Surgery
  • •Major Neurological Disease
  • •Gross Cognitive Dysfunction
  • •Patients not expected to be able to complete the 1 week and 3 months post-operative visit.

Arms & Interventions

Cerebral Desaturation, i.e; SctO2 < 60 % for 5 minutes

Active Comparator

Once the cerebral desaturation is established, the study personnel will attempt to optimize the level of oxygen within the brain of the study patients.

Intervention: SctO2 < 60 %. (Procedure)

Patients with SctO2 less than 60 %.

No Intervention

The study patients will not get any intervention in this arm if the Sct02 falls below 60%

Outcomes

Primary Outcomes

The association of Postoperative Delirium (PD) and Postoperative Cognitive Dysfunction (POCD) with changes in cerebral tissue oxygen saturation (SctO2).

Time Frame: First 5 days after the cardiac surgery.

Secondary Outcomes

  • Postoperative Morbidity and Mortality(3 months postoperatively)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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