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NCT06750497Recruiting

Forearm Immobilization in T2D

The Impact of Short-term Forearm Immobilization on Forearm Muscle Glucose and Amino Acid Metabolism of Volunteers With or Without Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 2 Jul 2026

Brief summary (registry, in English)

The aim of the present study is to assess the impact of short-term forearm immobilization on forearm muscle glucose uptake and amino acid net balance and kinetics in individuals with T2D compared with a control group with normoglycaemia.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
26 (estimated)
First submitted
22 Nov 2024
Start date
21 Nov 2024
Primary completion date
30 Apr 2027
Lead sponsor
Wageningen University
NCT number
NCT06750497

What you commit to

  • Study type: Interventional
  • Planned participants: 26
  • From 21 Nov 2024 to the primary completion date, 30 Apr 2027
  • 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

  • Chronic use of any prescribed or over-the-counter pharmaceuticals (excluding oral contraceptives and contraceptive devices) that interact with muscle substrate metabolism (e.g. selective serotonin reuptake inhibitors)
  • Any previous motor disorders or inborn errors in muscle and/or lipid metabolism

Other illness

  • Type 1 or a genetic form of diabetes
  • Any diagnosed cardiovascular (heart) disease or high blood pressure (≥160 mmHg systolic and/or ≥100 mmHg diastolic)
  • A personal or family history of thrombosis (clots)
  • History of kidney disease
  • History of liver disease
  • History of any drug or alcohol abuse in the past two years

Other

  • Consumption of a low-carbohydrate diet
  • Smoking or chewing tobacco
  • Known anaemia
  • Regular use of dietary protein and/or amino acid supplements (\>3 times per week)
  • Currently involved in a structured progressive resistance training program (\>3 times per week)
  • Pregnant or breastfeeding
  • Claustrophobia
  • Unable to give consent

Who the study is looking for

  • Males and females with or without diagnosed type 2 diabetes
  • Use lifestyle changes, metformin, gliclazide, or a combination thereof as oral glucose-lowering treatments for T2D
  • Aged 18-80 years at the time of signing informed consent
  • 18.5 ≥ BMI ≤ 35 kg·m2

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Wageningen University and Research
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WageningenNetherlandsRecruiting

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