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Clinical Trials/NL-OMON40429
NL-OMON40429
Completed
Not Applicable

Predicting postoperative outcome in elderly surgical cancer patients - Biomarkers and handgrip strength as predictors of postoperative outcome in elderly - PICNIC B-HAPPY

niversitair Medisch Centrum Groningen0 sites672 target enrollmentTBD
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Conditions1) Postoperative cognitive dysfunction 2) functionloss after surgerymemory- and concentrationproblems and loss of ability to handle daily activities100098411000147410017998

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
1) Postoperative cognitive dysfunction 2) functionloss after surgery
Sponsor
niversitair Medisch Centrum Groningen
Enrollment
672
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Patients over 65 years of age undergoing surgery for a solid malignancy.
  • •Surgery is scheduled more than 24 hours after inclusion in the study as we feel this is the time necessary to obtain test results and plan the intraoperative recording of data.
  • •Surgery under general, local or regional anesthesia.
  • •Written informed consent given according to local regulations.
  • •Patients can only be included in this trial once.;Control group:
  • •Patients \<65 years of age undergoing surgery for a solid malignancy.

Exclusion Criteria

  • •Any physical condition potentially hampering compliance with the study protocol and follow\-up schedule, this includes: severe visual impairment, total deafness or the inability to hold a pencil.
  • •Personal time constraints unabling patients to comply to the study protocol.
  • •Patients unable to comply with the outcome questionnaires (this includes insufficient knowledge of the Dutch language).

Outcomes

Primary Outcomes

Not specified

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