- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03785275
Beta Cell Imaging in T1D Patients With a Different Glycemic Control (GLP1-reg)
29. januar 2022 opdateret af: Radboud University Medical Center
Beta Cell Imaging in Type 1 Diabetes With Stable Near-normal and Unstable Glucose Control Using PET
The primary aim of this study is to measure (residual) beta cell mass in type 1 diabetes (T1D) patients with stable near-normal and unstable glucose control using PET/CT imaging, to improve the understanding of the relation between beta cell mass and glycemic control in T1D.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Type 1 diabetes (T1D) is characterized by a progressive decrease in beta cell function due to an autoimmune attack on the beta cells, which will lead to a reduction in insulin secretion.
Endogenous insulin secretion can be determined measuring C-peptide, which is secreted in equal amounts to insulin.
The loss of insulin secretion, indicated by an immeasurable C-peptide level, will hamper glycemic control which results in increased glycated haemoglobin (HbA1c) levels.
Also, hypoglycemic events can occur more frequently.
Initially, the belief was that this could be explained by the loss of all pancreatic beta cells due to the autoimmune attack.
However, recent literature suggests that a considerable number of beta cells can survive this attack.
This could mean that certain beta cells survived, but have lost their function.
The ratio of functional and non-functional residual beta cells might play an important role in the degree of glycemic control.
It would therefore be of great interest to study residual beta cell mass in two types of T1D patients that differ in glycemic control.
Although both types of patients receive treatment, one group of patients is characterized by a stable near-normal glucose control while the second group is characterized by an unstable glucose control.
In case glycemic control mostly depends on beta cell function and less on beta cell mass, novel therapies could focus on the functional reactivation of these non-functional beta cells to restore overall beta cell function.
This could especially be in favour of patients with an unstable glucose control.
Beta cell mass will be determined using Ga-68-NODAGA-exendin-4 positron emission tomography (PET), which allows visualization of pancreatic beta cells as well as absolute quantification of tracer uptake, providing a measure for the pancreatic beta cell mass.
The outcome of this study will lead to a better understanding of the relation between the amount of residual beta cells, beta cell function and the influence of glycemic control.
This could provide new insights regarding the development of new therapies to improve beta cell function and glycemic control, which could lower disease burden and improve the patient's quality of life.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
16
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Gelderland
-
Nijmegen, Gelderland, Holland, 6525 GA
- Radboudumc
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
The study population will include 18 individuals with T1D for at least 1 year with a minimum age of 18 years.
This population consists of two groups that include 9 subjects with stable near-normal glucose control and 9 individuals with unstable glucose control.
The differentiation between T1D patients with stable near-normal and unstable glucose control will be based on their HbA1c value, the number of severe hypoglycemic events and the patient's hypoglycaemic awareness.
Beskrivelse
Inclusion Criteria:
Group 1 (stable glycemic control)
- Age ≥18 years
- T1D diagnosed ≥1 year at the start of the study
- HbA1c <7 (<53 mmol/mol)
- 17≤ BMI ≤30 kg/m2
- No severe hypoglycemic events in the past year and a maximum of 2 severe hypoglycemic events in their entire life.
- Intact hypoglycemic awareness
- Ability to sign informed consent
Group 2 (unstable glycemic control) Age ≥18 years
- T1D diagnosed ≥1 year at the start of the study
- HbA1c >8.5 (>69 mmol/mol)
- 17≤ BMI ≤30 kg/m2
- Minimum of 2 severe hypoglycemic events in the past year, or an impaired awareness of hypoglycemia (subjects may comply with both criteria, but this is not a requirement)
- Ability to sign informed consent
Exclusion Criteria:
- Previous treatment (within 6 months) with synthetic Exendin (Exenatide, Byetta®) or Dipeptidyl-Peptidase IV inhibitors
- Liver disease
- Renal disease
- Pregnancy or the wish to become pregnant within 6 months after the study
- Breastfeeding
- BMI <17 kg/m2 or BMI >30 kg/m2
- Age <18 years
- Inability to sign informed consent
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Subjects with stable near-normal T1D
|
PET/CT scan after injection with gallium-68-exendin
|
|
Subjects with unstable T1D
|
PET/CT scan after injection with gallium-68-exendin
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Beta cell mass
Tidsramme: 2 years
|
Pancreatic uptake of the tracer is measured by quantitative analysis (measure for beta cell mass)
|
2 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Beta cell mass vs. beta cell function
Tidsramme: 2 years
|
The correlation of the measured beta cell mass to the beta cell function
|
2 years
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
6. december 2017
Primær færdiggørelse (Faktiske)
9. november 2020
Studieafslutning (Faktiske)
9. november 2020
Datoer for studieregistrering
Først indsendt
20. december 2018
Først indsendt, der opfyldte QC-kriterier
21. december 2018
Først opslået (Faktiske)
24. december 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
14. februar 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
29. januar 2022
Sidst verificeret
1. januar 2022
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- NL59582.091.17
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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Ingen
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