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Clinical and Biological Sample Database of Chinese Elderly Patients With Multiple Diseases

Capital Medical University logo

Capital Medical University

Status

Enrolling

Conditions

Comorbidities and Coexisting Conditions
Old Age; Debility

Study type

Observational

Funder types

Other

Identifiers

NCT05797402
2020YFC2004800

Details and patient eligibility

About

The investigators aim to establish a clinical database and biobank for elderly patients with multiple diseases. The collected data will include demographic information, comorbidity characteristic, FRAIL scale, age-adjusted Charlson comorbidity index, relevant blood tests, the results of imaging examination, prescription of drugs, length of hospital stay, number of overall rehospitalizations and death. With this database, the investigators intend to formulate an individualized treatment strategy for these patients.

Full description

According to the China Health and Aging Tracking Survey, a significant proportion of elderly individuals aged over 65 suffer from two or more chronic diseases, with prevalence rates ranging from 22.5% to 47.5%. However, due to the decentralized storage of health data, lack of standardization, and collaboration barriers, it is challenging to make use of this information in a meaningful way.Therefore, there is an urgent need to overcome the technical challenges and build an intelligent diagnosis and treatment system for this vulnerable population.

To achieve this goal, it is necessary to establish a clinical database and biobank that includes data on all elderly patients with multimorbidity. This will enable researchers to conduct clinical research on various factors, including clinical and biological predictors of adverse events such as emergency visits, strokes, heart failure, myocardial infarction, tumors, and acute chronic obstructive pulmonary disease. Additionally, the database will facilitate the development of systematic and individualized evaluation tools for elderly patients with multimorbidity, identify prognostic factors that improve short- and long-term outcomes, and enable the participation in multi-center trials at the national or international level. Ultimately, this effort will help establish clinical database and biobank data collection standards for future studies.

Enrollment

10,000,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • (1) written and informed consent, (2) participants aged 18 years or older.

Exclusion criteria

  • (1) Unwilling to participate in the study, (2) Unable or unwilling to cooperate with the baseline or follow-up data collection.

Trial design

10,000,000 participants in 3 patient groups

young-aged patients
Description:
Patients aged 18 to 45 years old.
middle-aged patients
Description:
Patients aged 46 to 64 years old.
elderly patients
Description:
Patients aged 65 and older.

Trial contacts and locations

1

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Central trial contact

Shao-ping Nie, MD,PhD

Data sourced from clinicaltrials.gov

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