NCT07599072Recruiting
PREdiabetes GLycemic Impact and Data Evaluation
Evaluation of the Impact of Continuous Glucose Monitoring (CGM) Systems on Glycemic Control in People With Prediabetes: Postmarketing Clinical Study
Source: ClinicalTrials.gov · Last updated 29 Sept 2026
Brief summary (registry, in English)
This prospective, randomized controlled trial evaluates whether real-time continuous glucose monitoring (CGM) improves glycemic control and lifestyle adherence in adults with prediabetes compared to conventional self-monitoring methods over a 3-month period. By analyzing metabolic markers and behavioral data, the study aims to determine the effectiveness of 24-hour monitoring as a personalized tool that increases patient adherence to lifestyle changes compared to conventional SMBG methods.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- First submitted
- 14 May 2026
- Start date
- 1 Jul 2026
- Primary completion date
- 31 May 2027
- Lead sponsor
- Nazarii Kobyliak
- Diseases
- Obesity
- NCT number
- NCT07599072
What you commit to
- Study type: Interventional
- Planned participants: 80
- From 1 Jul 2026 to the primary completion date, 31 May 2027
- 3 sites 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
- Daily use of any form of steroid medication (oral, inhaled, injected) within the last 3 months;
Other illness
- Presence of type 1 or type 2 diabetes;
- Active cardiovascular diseases within 12 months of Visit 1, such as myocardial infarction, clinically significant arrhythmia, unstable angina, coronary artery bypass surgery, or angioplasty; or are expected to require coronary artery bypass surgery or angioplasty during the course of the study;
- Endocrine disorders (e.g., Itsenko-Cushing syndrome, acromegaly) that affect glycemia;
- Known allergy to sensor materials;
- Has evidence of current abuse of drugs or alcohol or a history of abuse that, in the investigator's opinion, would cause the individual to be noncompliant;
Lab values
- Decompensated liver or kidney diseases (GFR \< 45 ml/min/1. 73 m²);
Other
- Pregnancy or lactation;
- Mental or cognitive impairments that would interfere with study participation;
- Recent use of any CGM within the last 12 months;
- Participation in another clinical study within the last 3 months.
Who the study is looking for
- Age of 18 years and older.
- Presence of prediabetes diagnosed according to criteria of the American Diabetes Association
- Persons who treated with diet and exercise alone or metformin on a stabilized dose for at least 3 months before the study;
- Ability to comply with protocol requirements and maintain a patient diary.
- Signed informed consent.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Hospital of Bogomolets National Medical University Coordinator of this site? Confirm its status | Kyiv | Ukraine | Recruiting |
| Bogomolets National Medical University Coordinator of this site? Confirm its status | Kyiv | Ukraine | Recruiting |
| Bogomoletz Institute of Physiology Coordinator of this site? Confirm its status | Kyiv | Ukraine | Enrolling by invitation |
This page is information, not medical advice. Discuss any trial with your doctor.