Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 11:11 AM
Ignite Modification Date:
2025-12-26 @ 11:11 AM
NCT ID:
NCT06862128
Eligibility Criteria:
Inclusion Criteria:
* Prediabetes indicated by ≥2 of the following values, measured at separate occasions or through different analyses during the past 2 years:
* \- Fasting venous plasma glucose ≥6.1 but ≤6.9 mmol/L
* \- Non-fasting venous plasma glucose ≥7.8 but ≤11.0 mmol/L
* \- HbA1c ≥39 but ≤47 mmol/mol
* Access to a smart phone which is compatible with the CGM application and has working Bluetooth connectivity
* Ability to read and respond to online instructions and questionnaires in Swedish.
Exclusion Criteria:
* T2D indicated by ≥2 of the following values, measured at different occasions or through different analyses:
* \- Fasting venous plasma glucose ≥7.0 mmol/L
* \- Non-fasting venous plasma glucose value ≥11.1 mmol/L
* \- HbA1c ≥48 mmol/mol
* Previous bariatric surgery e.g., gastric by-pass or gastric sleeve surgery
* Body mass index \<20 kg/m2
* Body weight \<43 kg
* Current pregnancy
* Need of regular use of GLP-1 receptor agonists, SGLT-2 inhibitors, acetaminophen or ascorbic acid supplements during the study period
* Fear of needle sticks
* Shift work during the study period
* Involvement in the study design, data collection, analysis, or participant recruitment.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
70 Years
Study:
NCT06862128
Study Brief:
Protocol Section:
NCT06862128