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China Adrenal Disease Registry (CASE)

S

Shanghai Jiao Tong University School of Medicine

Status

Enrolling

Conditions

Adrenal Carcinoma
Adrenal Adenoma
Congenital Adrenal Hyperplasia
Aldosteronism
Cushing Syndrome
Hypoadrenalism
Adrenal Incidentaloma
Pheochromocytoma

Study type

Observational

Funder types

Other

Identifiers

NCT04890444
Ruijin-adrenal01

Details and patient eligibility

About

Epidemiologic studies have revealed a tremendous increase in the prevalence of adrenal associated disease and related mortality worldwide. In order to meet all the therapeutic challenges in adrenal disease in China, CASE was founded in 2020. The objective of CASE is to launch an adrenal disease management model based on the Internet health information platform which allows the application and evaluation of adrenal disease treatment strategies at multiple centers. The proprietary electronic medical database will help the dynamic big-data analysis in epidemiology of adrenal disease, diagnosis, and treatment.

Full description

In order to meet all the challenges in the diagnosis and treatment of adrenal diseases in China, CASE was founded in 2020. With advanced medical equipment and Internet of Things (IoT) technology, CASE is committed to creating an online and offline integrated solution for adrenal disease, and for the entire spectrum of adrenal disease, to achieve a more convenient and precise model of care for patients, aiming to establish a platform with diagnosis and treatment of adrenal disease and their long-term follow-up. It allows the application and evaluation of treatment strategies at these centers.

Enrollment

2,000 estimated patients

Sex

All

Ages

16 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age ≥ 16 years old and ≤ 75 years
  2. Patients diagnosed with adrenal associated diseases, including cushing syndrome, primary aldosteronism, primary hypoadrenalism, congenital adrenal hyperplasia and adrenal adenomas, incidentalomas, and carcinomas, pheochromocytoma, etc.
  3. Provide written informed consent
  4. Satisfactory compliance

Exclusion criteria

  1. Patients with significantly reduced life expectancy (less than 2 years)
  2. With Drug abuse
  3. With AIDS or syphilis or infectious diseases such as viral tuberculosis in active phase at enrollment

Trial contacts and locations

1

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Central trial contact

shouyue SUN, MD

Data sourced from clinicaltrials.gov

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