- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT00639613
The Role of Small Intestinal Endocrine Cells in Type 2 Diabetic Hyperglucagonemia (T2DM-PC1-2)
25 juni 2015 uppdaterad av: Filip Krag Knop, University Hospital, Gentofte, Copenhagen
Exspression of Prohormone Convertase 1 and 2 in Small Intestinal Endocrine Mucosa Cells in Patients With Type 2 Diabetes
The purpose of this study is to determine whether excessive secretion of glucagon in type 2 diabetes originates from the pancreatic alpha-cells or endocrine cells in the mucosa of the small intestinal.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Hyperglucagonemia contributes significantly to the hyperglycemia characterizing patients with Type 2 diabetes.
Fasting hyperglucagonemia induces hepatic glucose release resulting in elevated fasting levels of plasma glucose.
Furthermore, lack of postprandial suppression of glucagon secretion - exchanged for a paradoxical postprandial hypersecretion of glucagon - results in increased levels of postprandial plasma glucose.
Additionally, type 2 diabetes is characterized by decreased postprandial responses of the insulinotropic (and glucagonostatic) peptide hormone glucagon-like peptide-1 (GLP-1).
Recent studies from our group suggest that the intestines are involved in the diminshed suppression of glucagon following ingestion of nutrients.
Thus, suppression of glucagon during oral glucose ingestion diminishes and reverses to stimulation while suppression during intravenous administered glucose sustains along with development of glucose intolerance.
In the small intestines mucosal endocrine L-cells secrete GLP-1, which is processed from its precursor, proglucagon, by prohormone convertase 1 (PC1).
In the pancreatic alpha-cells proglucagon is processed to glucagon via prohormone convertase 2 (PC2).
We plan to examine biopsies from the mucosa of the small intestines from patients with type 2 diabetes and from healthy subjects for glucagon production.
Furthermore, the volunteers will be subjected to a standard meal test in order to correlate the gene expression studies with the level of postprandial hyperglucagonemia of the subjects.
Studietyp
Observationell
Inskrivning (Faktisk)
20
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Copenhagen County
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Hellerup, Copenhagen County, Danmark, 2900
- Department of Internal Medicine F' laboratory
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
35 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Allt
Testmetod
Icke-sannolikhetsprov
Studera befolkning
Patients with type 2 diabetes
Beskrivning
Inclusion Criteria:
- Diagnosed with type 2 diabetes for at least 3 months
- Normal hemoglobin
- Informed consent
Exclusion Criteria:
- Liver disease (ALAT/ASAT > 2 x normal range)
- Diabetic nephropathy (se-creatinin > 130 µM and/or albuminuriu)
- Treatment with medication that can not be stopped for12 hours
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
|---|---|
|
2
Friska ämnen
|
Double-balloon enteroscopy allows for the entire gastrointestinal tract to be visualized in real time.
The technique involves the use of a balloon at the end of a special enteroscope camera and an overtube, which is also fitted with a balloon.
The procedure is usually done with the use of conscious sedation.
The enteroscope and overtube are inserted through the mouth and passed in conventional fashion (that is, as with gastroscopy) into the small bowel.
Following this, the endoscope is advanced a small distance in front of the overtube and the balloon at the end is inflated.
Using the assistance of friction at the interface of the enteroscope and intestinal wall, the small bowel is accordioned back to the overtube.
The overtube balloon is then deployed, and the enteroscope balloon is deflated.
The process is then continued until the entire small bowel is visualized.
Double-balloon enteroscopy allows for the sampling or biopsying of small bowel mucosa.
Liquid meal consisting of 100 g "Ny NAN" dissolved in 300 ml water (ca.
5000 kJ) to be ingested over 5 minutes.
Blood will be sampled for 4 hours following ingestion.
Samples are centrifuges and plasma will be analysed for glucagon, GLP-1, GIP, insulin and C-peptide concentrations.
|
|
1
Patients with type 2 diabetes
|
Double-balloon enteroscopy allows for the entire gastrointestinal tract to be visualized in real time.
The technique involves the use of a balloon at the end of a special enteroscope camera and an overtube, which is also fitted with a balloon.
The procedure is usually done with the use of conscious sedation.
The enteroscope and overtube are inserted through the mouth and passed in conventional fashion (that is, as with gastroscopy) into the small bowel.
Following this, the endoscope is advanced a small distance in front of the overtube and the balloon at the end is inflated.
Using the assistance of friction at the interface of the enteroscope and intestinal wall, the small bowel is accordioned back to the overtube.
The overtube balloon is then deployed, and the enteroscope balloon is deflated.
The process is then continued until the entire small bowel is visualized.
Double-balloon enteroscopy allows for the sampling or biopsying of small bowel mucosa.
Liquid meal consisting of 100 g "Ny NAN" dissolved in 300 ml water (ca.
5000 kJ) to be ingested over 5 minutes.
Blood will be sampled for 4 hours following ingestion.
Samples are centrifuges and plasma will be analysed for glucagon, GLP-1, GIP, insulin and C-peptide concentrations.
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Utredare
- Huvudutredare: Filip K Knop, MD PhD, Department of Internal Medicine
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 mars 2008
Primärt slutförande (Faktisk)
1 juni 2015
Studieregistreringsdatum
Först inskickad
12 mars 2008
Först inskickad som uppfyllde QC-kriterierna
12 mars 2008
Första postat (Uppskatta)
20 mars 2008
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
26 juni 2015
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
25 juni 2015
Senast verifierad
1 juni 2015
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- H-B-2007-031
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .