Patient-Centred Outcomes and Resource Utilisation After Noncardiac Surgery-D(Eutschland) (PACORUS-D)

NCT04675905 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1200

Last updated 2020-12-19

No results posted yet for this study

Summary

The PACORUS-D project aims at 1) quantifying the 30-days and 1-year disability burden (assessed using the 12-item WHODAS 2 \[WHO Disability Assessment Schedule\] questionnaire) after inhospital noncardiac nonneurosurgical procedures ; 2) quantifying the resource utilization up the 1 year after inhospital noncardiac nonneurosurgical procedures; 3) validating days alive and out of hospital (construct and criterion validity) in Germany. PACORUS-D consists of 2 independent cohort: a clinical multicentre cohort to assess "disability" and "days alive and out of hospital" and an administrative cohort to assess "days alive and out of hospital" and "resource utilization" from statutory health insurance data. PACORUS-D is intended as preparatory project in Germany before international expansion. THIS REGISTRATION REFERS TO THE CLINICAL COHORT ONLY.

Conditions

  • Noncardiac Surgery

Interventions

OTHER

no intervention (cohort study)

Explanatory variables include preoperative comorbidities, baseline disability, surgical risk, postoperative complications, sex, rural/urban area of residency, Oslo Social Support Scale; Clinical Frailty Scale in patients aged \>= 65 years

Sponsors & Collaborators

  • Heinrich-Heine University, Duesseldorf

    collaborator OTHER
  • University Hospital, Bonn

    collaborator OTHER
  • University Hospital, Aachen

    collaborator OTHER
  • University Hospital of Cologne

    collaborator OTHER
  • University Hospital, Essen

    collaborator OTHER
  • University Hospital Heidelberg

    collaborator OTHER
  • Ruhr University of Bochum

    collaborator OTHER
  • German Society of Anesthesiology and Intensive Care (DGAI)

    collaborator UNKNOWN
  • PD Dr. med. MSc Giovanna Lurati Buse

    lead OTHER

Principal Investigators

  • Giovanna AL Lurati Buse, MD, MSc · Anesthesiology Department, University Hospital Düsseldorf

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-02-01
Primary Completion
2022-10-31
Completion
2022-10-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04675905 on ClinicalTrials.gov