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Clinical Trials/NCT01316965
NCT01316965
Terminated
N/A

CONFUCIUS Study : Impact of a Multifaceted Program to Prevent Postoperative Delirium in the Elderly

Hospices Civils de Lyon1 site in 1 country175 target enrollmentApril 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Postoperative Delirium
Sponsor
Hospices Civils de Lyon
Enrollment
175
Locations
1
Primary Endpoint
Postoperative delirium rate within 7 days after surgery
Status
Terminated
Last Updated
8 years ago

Overview

Brief Summary

Postoperative delirium is common in the elderly and is associated with a significant increase in mortality, complications, length of hospital stay and admission in long care facility. Several interventions have proved their effectiveness to prevent it but their combination within a multifaceted intervention needs to be assessed using rigorous methodology based on randomized study design. CONFUCIUS trial aims to measure the impact of a multifaceted program on the prevention of postoperative delirium in elderly.

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
May 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female subject aged over 75 years
  • Admission for a scheduled surgery (i.e. all oncologic digestive surgery , ureterostomy, nephrectomy or cystectomy, total hip or knee replacement)
  • Participation agreement

Exclusion Criteria

  • Patients with a progressive and/or poorly managed psychiatric pathology (patients with stabilized depression could be included in the study)

Outcomes

Primary Outcomes

Postoperative delirium rate within 7 days after surgery

Time Frame: 7 days after surgery

Secondary Outcomes

  • Length of hospital stay(Hospital discharge)
  • Mortality 6 months after surgery(6 months after surgery)
  • Mean delirium intensity within 7 days after surgery(7 days after surgery)
  • Postoperative complications 30 days after surgery incidence(30 days after surgery)
  • Feasibility of the multidisciplinary prevention program(24 months)

Study Sites (1)

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