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Surveillance of High-risk Early Postsurgical Patients for Real-time Detection of Complications

NCT02957825 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 747

Last updated 2023-11-21

No results posted yet for this study

Summary

The aim of this study is to test the hypothesis that continuous wireless monitoring on the postsurgical ward will improve patient outcome, measured as disability-free survival at three months after surgery. Further, the investigators hypothesize that this tight control regimen decreases length of hospital stay and treatment costs in patients with complications.

Conditions

  • Complication, Postoperative

Interventions

DEVICE

Continuous wireless monitoring

Continuous wireless monitoring of vital signs

Sponsors & Collaborators

  • UMC Utrecht

    collaborator OTHER

  • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

    lead OTHER

Principal Investigators

  • Benedikt Preckel, MD · Academic Medical Centyer Amsterdam, Anesthesiology

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-02
Primary Completion
2021-08-31
Completion
2021-08-31

Countries

  • Netherlands

Study Locations

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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 NCT02957825 on ClinicalTrials.gov