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Perioperative Continuous Glucose Monitoring in Patients Undergoing an Abdominal Surgery

NCT03935919 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2020-04-08

No results posted yet for this study

Summary

The purpose of this study it to assess whether the continuous glucose monitor system Dexcom G6® can be reliably used for perioperative glucose monitoring in 20 prediabetic or diabetic patients undergoing abdominal surgery in terms of data continuity, accuracy and patient tolerability.

Conditions

Sponsors & Collaborators

  • Insel Gruppe AG, University Hospital Bern

    lead OTHER

Principal Investigators

  • Lia Bally, MD PhD · Inselspital, University Hospital of Bern, University of Bern

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-13
Primary Completion
2020-02-26
Completion
2020-03-01

Countries

  • Switzerland

Study Locations

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Entities

Diseases

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 NCT03935919 on ClinicalTrials.gov