Recruiting NA Type 2 Diabetes

Tests treatment safety and results for Type 2 Diabetes

Official title Effects and Safety of Diabetic GUideline Algorithm Implementation Performed by Primary Care Physicians in the Community

ClinicalTrials.gov ID: NCT05349955

What this study is testing

What it's testing
The Effects and Safety of Diabetic GUideline Algorithm Implementation in the Community (GUARD-Community) study is a 2-arm, cluster-randomized control trial to evaluate the effect and safety of guideline algorithm intervention performed by primary care physicians on cardiovascular and renal outcomes in elderly patients with high risk in community.
  • Time commitment: about 4 years
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 65 and older

You may be able to join if

  • ①Males or females aged 65 and above (≥65) receive treatment from the local community health service center;
  • ②Diagnosed type 2 diabetes (ADA criteria):
  • A. Typical symptoms of diabetes + random blood sugar ≥ 11.1mmol/L;
  • B. Fasting blood glucose (FPG) ≥ 7.0mmol/L (fasting blood glucose is defined as no caloric intake within 8 hours);
  • C. Oral glucose tolerance test 2h blood glucose (OGTT) ≥ 11.1mmol/L (2h after meal);

You likely can't join if

  • ①Pregnant women or women planning to become pregnant;
  • ②eGFR\<30 mL/min/1.73m2 (CKD-EPI formula);
  • ③Patient cannot be followed up for 36 months (due to health condition or migration);
  • ④Unwilling or unable to sign the informed consent;
  • ⑤Type 1 diabetes;
See the full eligibility criteria
Who can join
  • ①Males or females aged 65 and above (≥65) receive treatment from the local community health service center;
  • ②Diagnosed type 2 diabetes (ADA criteria):
  • A. Typical symptoms of diabetes + random blood sugar ≥ 11.1mmol/L;
  • B. Fasting blood glucose (FPG) ≥ 7.0mmol/L (fasting blood glucose is defined as no caloric intake within 8 hours);
  • C. Oral glucose tolerance test 2h blood glucose (OGTT) ≥ 11.1mmol/L (2h after meal);
  • D. have been treated with antidiabetic drugs;
  • Each blood sugar test must be repeated to confirm the diagnosis;
  • ③Complicated with chronic kidney disease and/or very high/high risk of cardiovascular disease, meet any one of the following:
  • A. ASCVD, including coronary heart disease, cerebral infarction, peripheral vascular disease;
  • B. Or target organ damage (albuminuria, renal impairment with eGFR ≥ 30 ml/min/1.73m2, left ventricular hypertrophy or retinopathy);
  • C. ≥ 3 major risk factors (age ≥ 65 years old, hypertension, dyslipidemia, smoking, obesity );
  • D. Diabetes duration ≥ 10 years, with any one traditional cardiovascular risk factor such as advanced age, obesity, smoking, sedentary, family history of cardiovascular disease, hypertension, abnormal lipid metabolism.
What rules you out
  • ①Pregnant women or women planning to become pregnant;
  • ②eGFR\<30 mL/min/1.73m2 (CKD-EPI formula);
  • ③Patient cannot be followed up for 36 months (due to health condition or migration);
  • ④Unwilling or unable to sign the informed consent;
  • ⑤Type 1 diabetes;

The study team makes the final eligibility decision.

Where it's taking place

  • Suzhou, Jaingsu, China
  • Suzhou, Jiangsu, China

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The study runs about 4 years per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.

Who can join this trial?

This study is enrolling all sexes, 65 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Suzhou, Jaingsu, China; Suzhou, Jiangsu, China. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.