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N/A N=203

Postoperative Cognitive Dysfunction as Geriatric Syndrome

Cognitive Dysfunction

Enrolled (actual)
203
Serious AEs
Results posted
Feb 2025
Primary outcome: Primary: Postoperative Cognitive Dysfunction - Results of MMSE Before Operation — 79; 43; 37; 5 Participants — p=<0.0001

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
Tomas Bata Hospital, Czech Republic
Primary completion
Mar 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Postoperative Cognitive Dysfunction - Results of MMSE Before Operation
79; 43; 37; 5 <0.0001 sig
PRIMARY
Postoperative Cognitive Dysfunction - Results of MMSE After Operation
77; 43; 38; 6 < .001 sig
PRIMARY
Postoperative Cognitive Dysfunction - TEGEST Test Before Operation
40; 124 <0.0001 sig
PRIMARY
Postoperative Cognitive Dysfunction - TEGEST Test After Operation
77; 87 <0.001 sig
PRIMARY
Postoperative Cognitive Dysfunction -Clock Drawing Test Before Operation
21; 143 <0.001 sig
PRIMARY
Postoperative Cognitive Dysfunction - Clock Drawing Test After Operation
21; 143 <0.0001 sig
SECONDARY
Clinical Frailty Scale Before Operation
9; 43; 24; 23; 24; 22 <0.0001 sig
SECONDARY
Social Anamnesis Before Operation- Type of Accommodation
100; 40; 24 .562
SECONDARY
Social Anamnesis During Preanesthesia Exam - Living Situation
118; 46 0.129
SECONDARY
Social Anamnesis - Stairs or Elevator
53; 111 0.019 sig

Summary

This study is testing cognitive function before and after the surgery, with patient's informed consent. Patients of interest are 65 year or older, undergoing surgery in general or regional anesthesia. Investigators are using 3 tests. These are: MMSE (Mini Mental State Exam), TEGEST test (test of gestures) and Clock drawing test. Tests after surgery are performed 2 days until discharge. The testing is anonymous, patient is assigned a number. Main aim of this study is to find a suitable quick test of cognitive function for clinical practice before surgery in general or regional anesthesia.

Eligibility Criteria

Inclusion Criteria

  • age 65 or older
  • absence of sensory impairment (deafness)
  • full legal capacity
  • informed consent
  • ability to speak
  • elective or acute surgical procedure

Exclusion Criteria

  • somnolence, coma
  • sepsis
  • Glasgow coma scale 14 and less
  • known psychiatric disease
  • effect of premedication, drugs
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05648890). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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