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NCT04412798Completed

Orange Juice and Glycaemic Control in Type 2 Diabetes Mellitus

Impact of Orange Juice During Breakfast on Glycaemic Control in Individuals With Type 2 Diabetes Mellitus

Source: ClinicalTrials.gov · Last updated 17 May 2024

Brief summary (registry, in English)

The evidence on the consumption of 100% orange juice in people with type 2 diabetes is highly variable and largely out-of-date, with a few studies reporting acute negative glycaemic effects when 100% orange juice is drunk with or without a meal. The aim of the project is to study the impact of the intake of a single serving of 100% orange juice on glycaemic control in male patients with pre-existing type 2 diabetes mellitus. In addition, immunological parameters and Alzheimer disease related biomarkers will be assessed to examine the chronic inflammatory state of these patients

Status (registry)
Completed
Study type
Interventional
Enrollment
15 (actual)
First submitted
29 May 2020
Start date
1 May 2020
Primary completion date
1 Apr 2024
Lead sponsor
Hasselt University
NCT number
NCT04412798

What you commit to

  • Study type: Interventional
  • Participants enrolled: 15
  • From 1 May 2020 to the primary completion date, 1 Apr 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • participants on exogenous insulin therapy,

Other illness

  • participants with established cardiovascular disease,
  • neurological disease,
  • cancer,
  • renal disease.

Lab values

  • HbA1c \>8.5%,

Other

  • pregnancy,
  • BMI \<22 or \>35 kg/m²,
  • regular smokers (\>1 cigarette per day),
  • Participants who are unwilling to consume any of the standard foods/drinks

Who the study is looking for

  • Inclusion Criteria: individuals (aged 25-75 years) with up to 8 years of T2DM, according to ADA criteria (Two-hour plasma glucose ≥200 mg/dL (11.1 mmol/L) during OGTT. The test should be performed as described by the WHO, using a glucose load containing the equivalent of 75-g anhydrous glucose dissolved in water; or HbA1c \> ≥6.5% (48 mmol/mol)).

Age in the registry: 25 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hasselt University
Coordinator of this site? Confirm its status
HasseltBelgiumUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.