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

Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y Gastric Bypass: Comparing Tissue Glucose Levels Between Two Surgical Bypass Methods - a Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04172116
Enrollment
68
Registered
2019-11-21
Start date
2020-01-31
Completion date
2021-01-31
Last updated
2019-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Keywords

metabolic surgery

Brief 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.

Interventions

DEVICEContinuous glucose monitoring

see arm/group descriptions

Sponsors

Medtronic
CollaboratorINDUSTRY
Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who underwent bariatric-metabolic surgery at the Medical University of Vienna in the years 2012-2016 for the long and narrow pouch group 2. Patients who underwent bariatric-metabolic surgery at the Clinic of Hollabrunn in the years 2010- 2012 for the short and wide pouch group 3. Patients on oral medication for diabetes mellitus (for subgroup assessment) 4. Stable weight (not more than + 15kg from lowest weight postoperatively) 5. Stable BMI

Exclusion criteria

1. Unable to give written informed consent 2. Patients with methods other than RYGB 3. Reoperation within the observed period 4. Any intervention changing pouch size or diameter of the anastomosis after the initial operation 5. Known allergy to oral contrast agent 6. Any regular intake of medication interfering with blood glucose levels

Design outcomes

Primary

MeasureTime frameDescription
Tissue glucose levels6 daysDifference in tissue glucose levels after the two variations of the Roux-en-y Gastric bypass

Secondary

MeasureTime frameDescription
tissue vs. blood glucose levels1 dayComparison of tissue and blood glucose levels

Countries

Austria

Contacts

Primary ContactGerhard Prager, MD
gerhard.prager@muw.ac.at0043 40400 56210
Backup ContactJulia Jedamzik, MD
julia.jedamzik@muw.ac.at0043 40400 56210

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026