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OpenTrials
Completed

NCT Number: NCT01825148

GLP-1 Receptor Targeting in Diabetic and Healthy Individuals

The purpose of the study is to determine whether there are differences in pancreatic uptake of the radiotracer between healthy individuals and patients with type 1 diabetes. If T1D patients have a markedly reduced uptake, the compound may be suitable for estimation of pancreatic beta cell mass, i.e. the cells in the pancreas that produce insulin.

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Key information

Age range

21 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Radboud University Nijmegen Medical Center

Nijmegen, Gelderland, 6500 HB, Netherlands

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • type 1 Diabetes

Exclusion criteria

  • breast feeding
  • pregnant

Treatment and study plan

radiolabeled Exendin

Other

Primary outcomes

  1. pancreatic uptake of radiolabeled Exendin

    Time frame: 7 days

    uptake will be given as counts per MBq injected activity as determined by calibrated SPECT/CT scanner with attenuation correction.

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Registry information

Official study title

Clinical Proof-of-principle of the Determination of the Beta Cell Mass in Vivo by SPECT Imaging With the 111-In-labeled GLP-1 Analogue DTPA(Diethylenetriamine Pentaacetic Acid)-[K40]-Exendin 4

Acronym: GLP-1-CPOP

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Apr 5, 2013
Registry last updated
Dec 2, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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