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Clinical Trials/NCT02315846
NCT02315846
Completed
Not Applicable

Role of Acetylcholinesterase for the Diagnosis of Postoperative Delirium in Patients Needing Postoperative Monitoring

Heidelberg University1 site in 1 country120 target enrollmentJanuary 2014
ConditionsDelirium

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Delirium
Sponsor
Heidelberg University
Enrollment
120
Locations
1
Primary Endpoint
change of acetylcholinesterase (U/l)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The level of acetylcholinesterase is suspected to correlate with postoperative delirium. The investigators therefore score patients once preoperatively and twice postoperatively with the german version of the delirium-score NuDESC (Nursing Delirium Screening Scale) and compare the results with the acetylcholinesterase activity, butyrylcholinesterase activity and the serum anticholinergic activity (SAA) at corresponding time points.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
July 2014
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christoph Schramm, M.D.

Principal Investigator

Heidelberg University

Eligibility Criteria

Inclusion Criteria

  • Signed written informed consent
  • Elective surgery

Exclusion Criteria

  • Preexisting psychiatric or neurological disease
  • No surgery
  • Reduced level of consciousness

Outcomes

Primary Outcomes

change of acetylcholinesterase (U/l)

Time Frame: one day before surgery, 1-24h after surgery, 25-72h after surgery

change of acetylcholinesterase in units per litre

Secondary Outcomes

  • change of NuDESC(one day before surgery, 1-24h after surgery, 25-72h after surgery)
  • ICD-codes of coexisting diseases(25-72h after surgery)
  • change of medication(one day before surgery, 1-24h after surgery, 25-72h after surgery)
  • ICD-codes of main disease(25-72h after surgery)

Study Sites (1)

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