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Oral Glucosestimulation After Gastric Bypass Surgery

NCT01851616 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2013-05-10

No results posted yet for this study

Summary

The objective of this study is to examine gastric emptying and satiety hormones after oral glucose stimulation in 2 different concentrations in morbidly obese patients after Roux-en-Y-gastric-Bypass.

Conditions

Interventions

DIETARY_SUPPLEMENT

25g of glucose in 200ml tap water, given orally (plus 50 mg 13C-sodium acetate)

DIETARY_SUPPLEMENT

10g Glucose in 200ml tap water given orally (plus 50 mg 13C-sodium acetate)

Sponsors & Collaborators

  • University Hospital, Basel, Switzerland

    lead OTHER

Principal Investigators

  • Christoph Beglinger, Prof. · University of Basel

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2013-03-31
Completion
2013-04-30

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 NCT01851616 on ClinicalTrials.gov