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Precision Diabetes Management: Integrated East-West Approach

Construction of a Precision and Individualized Management Model for Diabetes With Integrated Traditional Chinese and Western Medicine

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07307040
Enrollment
2000
Registered
2025-12-29
Start date
2025-12-31
Completion date
2027-03-31
Last updated
2025-12-29

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

Conditions

Early-Onset Type 2 Diabetes

Keywords

Integrated Traditional Chinese and Western Medicine, Precision Management, Personalized Management, Early-Onset Type 2 Diabetes

Brief summary

This project will leverage a large-scale cohort of early-onset type 2 diabetes patients to conduct innovative prospective clinical research. By integrating traditional Chinese medicine diagnostic information, clinical data, laboratory results, continuous glucose monitoring, genetic information, multi-omics data, and multi-modal monitoring data, and utilizing advanced data analysis methods such as deep learning, the project aims to establish a comprehensive monitoring, precise classification, and personalized diagnosis and treatment model-a holistic management approach integrating traditional Chinese and Western medicine for early-onset type 2 diabetes. This initiative is expected to enhance the management of early-onset type 2 diabetes, improve treatment outcomes and quality of life for affected patients, pioneer an innovative path for personalized integrated traditional Chinese and Western medicine management in this population, and promote the application of precision medicine in diabetes prevention and treatment.

Interventions

OTHERNo interventions

No interventions

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years

Inclusion criteria

* The age at diabetes diagnosis is ≥18 years but \<40 years.

Exclusion criteria

* The clinical diagnosis was type 1 diabetes, and at the time of enrollment, antibody levels or insulin/C-peptide results still supported the original diagnosis. There were clear secondary factors contributing to hyperglycemia, such as Cushing's syndrome or pheochromocytoma.

Design outcomes

Primary

MeasureTime frame
Traditional Chinese Medicine Syndrome ScoreThrough study completion, an average of 3 months
HbA1cThrough study completion, an average of 3 months

Secondary

MeasureTime frame
Total CholesterolThrough study completion, an average of 3 months
TriglyceridesThrough study completion, an average of 3 months
Low-Density Lipoprotein CholesterolThrough study completion, an average of 3 months
Fasting Blood GlucoseThrough study completion, an average of 3 months
High-Density Lipoprotein CholesterolThrough study completion, an average of 3 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026