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Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y Gastric Bypass

NCT04172116 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 68

Last updated 2019-11-21

No results posted yet for this study

Summary

This study evaluates the difference in post prandial tissue glucose levels between two variation of Roux-en-Y Gastric bypass by continuous glucose monitoring.

Conditions

  • Continuous Glucose Monitoring
  • Roux-en-y Gastric Bypass
  • Hypoglycemia

Interventions

DEVICE

Continuous glucose monitoring

see arm/group descriptions

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Medical University of Vienna

    lead OTHER

Principal Investigators

  • Gerhard Prager, MD · Medical University of Vienna

Eligibility

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

Timeline & Regulatory

Start
2020-01-31
Primary Completion
2020-12-31
Completion
2021-01-31

Countries

  • Austria

Study Locations

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Diseases
Companies

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 NCT04172116 on ClinicalTrials.gov