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Recruiting NCT06320600

Precision Medicine of Diabetes Program in China

Observational Diabetes

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: no intervention.
Who it may be relevant to
Registry conditions: Diabetes. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The prevalence of diabetes has been increasing year by year. According to the International Diabetes Federation (IDF) statistics in 2021, the global number of people with diabetes has reached 537 million. The patient population is large and heterogeneous, and precise diagnosis and treatment of diabetes patients have been a focus of attention. The objective of this study is to clarify the current status of precision classification and diagnosis of diabetes patients through retrospective and prospective cohort studies, and to establish a model for precision classification and diagnosis of diabetes, improving the accuracy of diabetes classification and diagnosis; based on big data of precision medicine for diabetes patients and follow-up cohorts, to establish precise diagnostic, therapeutic, and predictive methods for diabetes; and through multi-omics data analysis, to explore the potential pathogenesis of diabetes, explaining the heterogeneity of patients, and guiding individualized treatment for patients.

Interventions

  • Other no intervention
    It's an observational study, no intervention included

Primary outcome measures

  • The currency analysis of diabetes classification [Time frame: July 1st 2023 to December 31th 2023]
Secondary outcome measures (3)
  • To establish a model for predicting diabetic retinopathy [Time frame: January 1st 2024 to December 31th 2028]
  • To establish a model for predicting diabetic kidney disease [Time frame: January 1st 2024 to December 31th 2028]
  • To establish a model for predicting diabetic neuropathy [Time frame: January 1st 2024 to December 31th 2028]

Eligibility criteria

Inclusion criteria

  • Patients diagnosed with diabetes according to WHO 1999 criteria

Exclusion criteria

  • with duration more than 1 year; Diabetes has not been diagnosed by WHO standards in 1999; Absence of medical history data

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • the Second Xiangya Hospital — Changsha

Identifiers

NCT: NCT06320600 · PDC

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗