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Copeptin Changes After Food Intake

Completed
Conditions
Healthy Adults
Copeptin
Registration Number
NCT01772914
Lead Sponsor
University Hospital, Basel, Switzerland
Brief Summary

The purpose of this study is to determine whether copeptin levels are affected by food intake.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Aged over 18 years
Exclusion Criteria
  • Intake of any kind of medication (except birth control pill)
  • BMI >30 kg/m2
  • Evidence of any acute illness
  • History of chronic illness
  • Pregnancy
  • Known galactosemia or maltose malabsorption
  • Baseline glucose level >5.5 mmol/l Baseline sodium level <135 mmol/l or >145 mmol/l

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in copeptin levels after intake of a oral glucose tolerance test- and a mixed meal tolerance test liquid30, 60, 90, 120, 180 minutes after intake of the test liquids
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University Hospital Basel

🇨🇭

Basel, Basel-Stadt, Switzerland

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