Skip to main content
Clinical Trials/NCT05406843
NCT05406843
Completed
Not Applicable

Postoperative Cognitive Dysfunction in Participants Undergoing Open Heart Surgery

Kocaeli University1 site in 1 country140 target enrollmentJanuary 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Cognitive Dysfunction
Sponsor
Kocaeli University
Enrollment
140
Locations
1
Primary Endpoint
Evaluation of postoperative cognitive functions in participants undergoing open heart surgery.
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

To determine the rate of Postoperative Cognitive Dysfunction (POCD) in the early and late postoperative periods by comparing the preop and postop period mini mental status tests in participants undergoing open heart surgery, and to compare the results of the investgators clinic with the world literature.

Detailed Description

Postoperative delirium (POD) and Cognitive Dysfunction (POCD) are changes in mental status, especially in the geriatric surgery population.Unlike other forms of delirium, POD results in early full recovery.Postoperative Cognitive Dysfunction (POCD) is more difficult to define and implies temporal consciousness impairment associated with surgery. While the diagnosis of delirium requires the detection of symptoms, the diagnosis of POCD requires preoperative neuropsychological testing and determining how much reduction will mean cognitive dysfunction. Postoperative delirium management is complex and requires multiple strategies. Methods of treating and preventing POCD are still uncertain.It is known that POCD is most commonly seen in patients undergoing open heart surgery.In this study, the investigators aim is to evaluate whether there is any change in cognitive status in the postoperative period compared to the preoperative period of participants who will undergo open heart surgery due to valve pathology or coronary stenosis.

Registry
clinicaltrials.gov
Start Date
January 1, 2020
End Date
August 1, 2021
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Huri Yeşildal

Assistant

Kocaeli University

Eligibility Criteria

Inclusion Criteria

  • 18-75 age
  • American Society of Anesthesiologists (ASA) II-III

Exclusion Criteria

  • Patients who died within 48 hours after the operation

Outcomes

Primary Outcomes

Evaluation of postoperative cognitive functions in participants undergoing open heart surgery.

Time Frame: 1 year

The aim is to understand whether there is a loss of cognitive functions in the postoperative period, according to the preoperative periods, by testing the participants with open heart surgery on the 3rd day, 7th day, and 2nd month after the surgery.

Secondary Outcomes

  • Comparison with the literature.(1 year)

Study Sites (1)

Loading locations...

Similar Trials