Type 2 Diabetes Trial, Recruiting NCT05706155 Sponsor: Hospital de Clinicas de Porto Alegre Condition: Type 2 Diabetes
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Type 2 Diabetes Trial, Recruiting

NCT05706155
Recruiting Not Applicable

Who may 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 might be able to join this trial:

  • Adults aged 18 to 65 years old
  • People who have been diagnosed with Type 2 Diabetes
  • People whose glycated hemoglobin (a measure of blood sugar control over time) is between 7% and 11%
  • People who are overweight or obese, with a BMI between 25 and 40
  • People who are currently taking diabetes medication (tablets or insulin) to lower blood sugar
  • People whose weight has been relatively stable (within about 5% variation) for at least 12 weeks before the screening visit
  • People who have not followed a formal diet program in the last 6 months
  • People who are able to understand and follow the study's activities and proposals
  • People who are willing and able to sign a written consent form and follow the study's requirements

Who may not be able to join:

  • People who have Type 1 diabetes
  • People who have eye disease (retinopathy) that affects their vision and limits their ability to participate in the study activities
  • People who have serious kidney disease (where kidney filtration is below a certain level)
  • People who have liver failure or chronic viral hepatitis (a liver infection)
  • People who have severe heart failure (Grade III or IV)
  • People who have an active or worsening brain or nerve disease (such as a neurodegenerative condition)
  • People who have had a stroke that left lasting effects
  • People who are taking medications that affect blood sugar levels or cause weight loss (for example, corticosteroids or immunosuppressants)
  • People who have taken steroid tablets or injections for more than 7 consecutive days within the 4 weeks before screening
  • People who have taken weight-loss medications (such as orlistat, sibutramine, topiramate, bupropion, liraglutide, or semaglutide) within the 12 weeks before screening
  • People taking thyroid hormone medication whose dose has not been stable for at least 12 weeks before screening
  • People who have had an active problem with substance misuse, including alcohol, within the last year
  • People whose thyroid stimulating hormone (TSH) level is outside the normal range
  • People with very high fasting triglyceride (a type of fat in the blood) levels of 600 mg/dL or above
  • People who have been diagnosed with or treated for cancer in the last 5 years (with some exceptions such as certain skin cancers — confirm with trial site)
  • People who have a serious psychiatric illness
  • People who have, or are at risk of, an eating disorder
  • Women who are pregnant, planning to become pregnant during the study, or currently breastfeeding
  • People who have had recent severe high blood sugar symptoms such as excessive thirst, frequent urination, or unexplained weight loss in the last 3 months
  • People who have experienced serious diabetes complications such as diabetic ketoacidosis or hyperosmolar coma
  • People the study investigators consider unlikely to complete the full study or be reliable participants
  • People who work night shifts finishing after 10pm
  • People who are currently following a vegetarian, vegan, or flexitarian diet
  • People who have previously had bariatric (weight loss) surgery
  • People who are living with HIV
  • People who have any other medical condition that investigators believe could interfere with their ability to complete the study or affect the safety and reliability of results
  • People who require any treatment during the study that could affect the study's results or the safety of the data collected

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 30 June 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Hospital de Clinicas de Porto Alegre
Registry
ClinicalTrials.gov
Start date
1 November 2022
Est. completion
30 December 2027

Where this trial is recruiting

🇧🇷 Brazil

Primary endpoints

Change in Glycated Hemoglobin

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: 30 June 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