Development of Perioperative Delirium Prediction Model

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorKubra Gunes

About this trial

Postoperative delirium is an acute organic brain dysfunction that is commonly observed following cardiovascular surgery. It presents with acute and fluctuating changes in the level of consciousness, resulting in impaired cognitive function and perception. The incidence of delirium following cardiac surgery has been reported to range from 11.4% to 55%. In light of the challenges associated with treating delirium once it has manifested, it is imperative to prioritise the early recognition and prevention of this condition. The objective of this study was to develop a perioperative delirium risk prediction model for patients undergoing cardiovascular surgery.

Eligibility criteria

Qualifiers

Over 18 years old

Previous cardiovascular surgery

No mental deficiency and visual and hearing impairment

Participants' acceptance to participate in the research

Disqualifiers

Cardiovascular surgery under emergency conditions

Being diagnosed with delirium, dementia, psychiatric illness and taking medication for this reason before the surgery

Serious conditions such as cardiopulmonary resuscitation during surgery

Alcohol and drug addiction

Trial design

Treatments tested in this trial

  • Group 1
  • Group 2

Treatment groups

770 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Kubra Gunes

Lead sponsor

Uludag University

Sponsor institution