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China Adrenal Disease Registry

China Adrenal Disease Registry Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04890444
Acronym
CASE
Enrollment
2000
Registered
2021-05-18
Start date
2021-06-01
Completion date
2026-04-30
Last updated
2022-02-14

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

Conditions

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

Brief summary

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.

Detailed 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.

Interventions

None listed

Sponsors

Shanghai Jiao Tong University School of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to 75 Years

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

Design outcomes

Primary

MeasureTime frame
Percentage of adrenal diseases in Chinathrough study completion, an average of 1 year
Number of participants with complication of adrenal diseases in Chinathrough study completion, an average of 1 year

Secondary

MeasureTime frameDescription
concentration of urine cortisolthrough study completion, an average of 1 year
concentration of androstenedionethrough study completion, an average of 1 year
concentration of adrenocorticotropic hormonethrough study completion, an average of 1 year
concentration of 17-hydroxyprogesteronethrough study completion, an average of 1 year
concentration of aldosteronethrough study completion, an average of 1 year
changes in adrenal CTthrough study completion, an average of 1 year
percentage of hypoadrenalismthrough study completion, an average of 1 year
Mental health statusthrough study completion, an average of 1 yearThe symptom checklist-90 will be used to evaluate the changes of participants' psychological state through study completion from 10 aspects, including somatization, obsessive-compulsive symptoms, interpersonal sensitivity, depression, anxiety, hostility, terror, paranoia, psychotic and others.
concentration of metanephrinesthrough study completion, an average of 1 year
concentration of cortisolthrough study completion, an average of 1 year

Countries

China

Contacts

Primary Contactshouyue SUN, MD
ssy10926@rjh.com.cn18121263206

Outcome results

None listed

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