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NCT00850928 · ClinicalTrials.gov registry record
Postoperative Cognitive Decline, Inflammation, and Plasma Levels of Beta-amyloids
A clinical trial, sponsored by NYU Langone Health.
- Completed
- Registry status
- 41
- Enrollment target
NCT00850928: Completed study, sponsored by NYU Langone Health.
NCT00850928 is a clinical trial that has completed, run by NYU Langone Health. The registered enrollment target is 41 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00850928 has completed, sponsored by NYU Langone Health.
- COMPLETED
- Registry status
- 41 participants
- Enrollment target
Study Summary
Postoperative cognitive dysfunction (POCD) can be a serious complication. The development of therapeutic strategies for the prevention and treatment of this condition requires the identification of subgroup of patients with the greatest incidence of POCD. Several retrospective analyses have raised the possibility that surgery is a risk factor for the accelerated progression of Alzheimer's disease (AD). Moreover, there is increasing evidence that inflammatory mechanisms are involved in the pathogenesis of AD. Major surgery can be associated with a profound systemic inflammatory response. Consequently, it is reasonable to suggest that there is a link between major surgery and the postoperative development of AD in patients who are already at high risk for this complication, e.g. the elderly with mild cognitive impairment. In addition, there are several laboratory investigations that suggest that anesthetic agents increase amyloid peptide levels as well as enhance oligomerization of these proteins. The significance of these findings, however, is unknown. This clinical study seeks to correlate perioperative inflammatory responses, perioperative changes in amyloid-beta protein levels (markers of AD) with neurocognitive and functional outcome in the elderly who are at risk for POCD. This knowledge does not exist, but is essential in the effort to plan perioperative care that can reduce the incidence of POCD as well as improve functional recovery.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 41 participants |
| Start Date | 2008-12 |
| Est. Completion | 2011-01 |
What the finished NCT00850928 record still lists
NCT00850928 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 41 participants, a relatively small participant target.
The record links to 0 conditions, and to 0 interventions.
NCT00850928 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00850928 about?
NCT00850928 is a clinical study titled "Postoperative Cognitive Decline, Inflammation, and Plasma Levels of Beta-amyloids". Postoperative cognitive dysfunction (POCD) can be a serious complication. The development of therapeutic strategies for the prevention and treatment of this condition requires the identification of subgroup of patients with the greatest incidence of POCD. Several retrospective analyses have raised t...
What is the current status of trial NCT00850928?
This trial is currently completed. The enrollment target is 41 participants. The study started on 2008-12. Estimated completion is 2011-01.
Who is sponsoring clinical trial NCT00850928?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
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