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Bestimmung der stimulierten ß-Zell-Kapazität im oralen Nateglinide 50 g Glukose-Toleranz-Test - „Nateglinide-Test“

Bestimmung der stimulierten ß-Zell-Kapazität im oralen Nateglinide 50 g Glukose-Toleranz-Test - „Nateglinide-Test“

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2006-006384-24-DE
Enrollment
Unknown
Registered
2007-03-16
Start date
2007-05-29
Completion date
Unknown
Last updated
2012-03-19

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

Conditions

Non-insulin demanding type 2 diabetes

Interventions

Trade Name: Nateglinide 120 mg Starlix 120 Pharmaceutical Form: Tablet INN or Proposed INN: NATEGLINIDE CAS Number: 105816044 Concentration unit: mg milligram(s) Concentration type: equal Concentratio

Sponsors

Johan Wolfgang Goethe Universität - Department of Internal medicine I, Division Endocrinology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Typ 2 Diabetes, male or female Age 18 – 80 years Control: young, healthy volunteers no diabetes, IFG or IGT stated in the case history Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Active, consuming diseases (cancer, HIV) Renal failure (creatinine >1,5 mg/dl) Liver diseases (AST, ALT >1,5x ULN) Psychiatric diseases Insulin therapy Pregnancy or missing contraception in childbearing ange, nursing contraindication to Nateglinide Typ 1 diabetes Unable or unwilling to comply with study Maltose-Malabsorption acut gastrointestinal infection gut surgery in the case history fever

Design outcomes

Primary

MeasureTime frame
Main Objective: Evaluation of the ß-cell-secretory-capacity by giving 120 mg Nateglinide and 50 g glucose in individuals with type 2 diabetes in a modyfied oral glucose tolerance test.;Secondary Objective: Classification of patients with type 2 diabetes;Primary end point(s): glucose, Insulin, C-peptide - AUC, - max. level and time of max. level Insulin resistence: HOMA-IR, QUICKI, ISI

Countries

Germany

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026