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Prevention of Postoperative Delirium After Acute Surgery (POD-CARE)

B

Bispebjerg Hospital

Status

Unknown

Conditions

Postoperative Delirium

Treatments

Other: Patient interventions
Other: Staff education

Study type

Interventional

Funder types

Other

Identifiers

NCT04857125
H-20067775

Details and patient eligibility

About

The aim of this trial is to evaluate the implementation and effect of an evidence based, multicomponent intervention on postoperative delirium, when fast implemented throughout the patients stay in hospital before, during and after acute surgery in a risk population, the primary outcome being frequency of patients with positive Confusion Assessment Method (CAM) score.

The hypothesis is that the frequency of postoperative delirium will be reduced after implementation of the preventive interventions.

Enrollment

476 estimated patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 40 or above.
  • Patients scheduled for acute abdominal or orthopaedic surgery in general anaesthesia with an expected duration of 30 minutes or more.
  • Patients who are scheduled for surgery within 72 hours of hospital admission.
  • Patients who are expected to stay in hospital for 24 hours or more.

Exclusion criteria

  • Patients screened CAM positive before surgery.
  • Patients who have already been included in the study
  • Patients unable to speak and read Danish.
  • Inability to provide consent.

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

Single Blind

476 participants in 2 patient groups

Multicomponent intervention
Active Comparator group
Description:
Pre-, intra- and postoperative interventions applied using the Fast-IM method.
Treatment:
Other: Staff education
Other: Patient interventions
Standard care
No Intervention group
Description:
Patients are receiving standard care.

Trial contacts and locations

1

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Central trial contact

Sine Eriksen, Cand. Cur.

Data sourced from clinicaltrials.gov

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