Type 2 Diabetes Trial, Recruiting NCT06752018 Sponsor: University of Aarhus Condition: Type 2 Diabetes
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Type 2 Diabetes Trial, Recruiting

NCT06752018
Recruiting Not Applicable

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who may be able to join

  • People who are willing and able to give spoken and written consent to take part in the study
  • Men and women aged 18 years or older
  • People whose body mass index (BMI) falls within a specific range — either 18.5–24.9 (lean/healthy weight range) for the control group, or 35–50 (higher weight range) for the group scheduled for gastric bypass surgery

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • People who are unwilling or unable to follow the study instructions
  • People who are pregnant
  • People with significant digestive or gut problems
  • People who use tobacco products
  • People who have consumed alcohol within two days before their study visit
  • People who have had an active cancer diagnosis within the past 5 years
  • People who use dietary supplements that affect inflammation (such as fish oil) and are not willing to stop taking them one week before their study visits
  • People who have an existing heart or metabolic condition, or who take medication related to such conditions (for example, blood pressure medication or insulin for diabetes)
  • People who have an existing inflammatory condition, or who take medication related to such a condition
  • People who have an increased tendency to bleed or who take blood-thinning medication
  • For the gastric bypass group only: people who have lost more than 8% of their body weight since being referred for surgery, or more than 3% of their body weight in the four months leading up to surgery

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 31 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Emma Börgeson, Dr., PhD, MSc, University of Aarhus

Phone: +45 9352 2984

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
30 January 2025
Est. completion
1 December 2030

Where this trial is recruiting

🇩🇰 Denmark

Primary endpoints

Whole blood ROS prooduction; Whole blood ROS production

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 31 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov