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Application of active diagnosis and treatment system based on artificial intelligence in the management of patients with type 2 diabetes mellitus: improving the comprehensive compliance rate of diabetes mellitus and improving the prognosis of diabetic retinopathy

Application of active diagnosis and treatment system based on artificial intelligence in the management of patients with type 2 diabetes mellitus: improving the comprehensive compliance rate of diabetes mellitus and improving the prognosis of diabetic retinopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124018
Enrollment
Unknown
Registered
2026-05-06
Start date
2026-05-06
Completion date
Unknown
Last updated
2026-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetesDiabetic retinopathy

Interventions

Active diagnosis and treatment group:Active diagnosis and treatment intervention
Control group:Traditional outpatient follow-up

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.The age is 18~75 years old (including the critical value, subject to the time when the informed consent form is signed); 2.Sex is not limited; 3.According to the diabetes diagnosis and classification criteria issued by the China Diabetes Prevention and Treatment Guidelines (2024 Edition), the diagnosis was type 2 diabetes; 4.Fully understand the purpose, nature, methods and possible adverse reactions of the experiment, voluntarily enter the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Combined with tumor, pregnancy, severe hepatic and renal insufficiency, acute cardiovascular and cerebrovascular diseases, etc; 2.Can't participate in follow-up regularly; 3.There are communication barriers and mental barriers; 4.Participants in other drug trials at present and in recent three months; 5.Any other circumstances that the researcher thinks may affect the patient's informed consent or compliance with the trial plan, or the patient's participation in the trial may affect the trial results or his own safety.

Design outcomes

Primary

MeasureTime frame
Comprehensive compliance rate (HbA1c<7%, blood pressure<130/80mmHg, LDL-C<2.6mmol/L, BMI<24kg/m^2).;DR early screening rate;

Secondary

MeasureTime frame
Changes in fasting weight and body mass index (BMI) from baseline;Medication compliance (minor program records missed doses);HbA1c compliance rate (proportion of subjects with HbA1c<7.0% and HbA1c<6.5%);Patient Satisfaction (Survey);Changes from baseline in dynamic blood glucose assessment indicators (Time in Target Range TIR, Standard Deviation of Blood Glucose SD, Maximum Glycemic Variation MAGE);Changes in systolic and diastolic blood pressures from baseline;Changes in fasting lipid profiles (TC, LDL-C, HDL-C, TG) from baseline;

Countries

China

Contacts

Public ContactQing Miao

Huashan Hospital, Fudan University

miaoqing@huashan.org.cn+86 21 52887027

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026