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Wireless Assessment of Respiratory and Circulatory Distress

NCT03491137 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 505

Last updated 2021-11-01

No results posted yet for this study

Summary

A high percentage of patients undergoing major abdominal surgery will develop a postoperative complication. Our hypothesis is that by observing postoperative patients with continuous wireless monitoring, it is possible to detect the correlation between deviating vital parameters and subsequent postoperative complications. A prospective observational study will take place on general surgical wards with the enrolment of 500 patients in two different hospitals. Physiological parameters will be recorded for 96 hours postoperative. Data is collected preoperative, peroperative and postoperative in up to 6 months for data analyzing.

Conditions

  • Postoperative Complications

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    collaborator OTHER

  • Technical University of Denmark

    collaborator OTHER

  • Danish Cancer Society

    collaborator OTHER

  • Bispebjerg Hospital

    lead OTHER

Principal Investigators

  • Camilla Haahr-Raunkjær, MD · Surgical department, Bispebjerg Hospital

  • Eske K Aasvang, Dr.med. · Abdominal surgical department, Rigshospitalet

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-22
Primary Completion
2020-08-30
Completion
2021-01-31

Countries

  • Denmark

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 NCT03491137 on ClinicalTrials.gov