China Adrenal Disease Registry
CASE
1 other identifier
observational
2,000
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 7, 2021
CompletedFirst Posted
Study publicly available on registry
May 18, 2021
CompletedStudy Start
First participant enrolled
June 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedFebruary 14, 2022
January 1, 2022
4.9 years
May 7, 2021
January 28, 2022
Conditions
Outcome Measures
Primary Outcomes (2)
Percentage of adrenal diseases in China
through study completion, an average of 1 year
Number of participants with complication of adrenal diseases in China
through study completion, an average of 1 year
Secondary Outcomes (10)
concentration of aldosterone
through study completion, an average of 1 year
concentration of cortisol
through study completion, an average of 1 year
concentration of urine cortisol
through study completion, an average of 1 year
concentration of androstenedione
through study completion, an average of 1 year
concentration of adrenocorticotropic hormone
through study completion, an average of 1 year
- +5 more secondary outcomes
Eligibility Criteria
This is an observational study. Participants enrolled in the study were diagnosed with adrenal associated diseases, including cushing syndrome, primary aldosteronism, primary hypoadrenalism, congenital adrenal hyperplasia and adrenal adenomas, incidentalomas, and carcinomas, pheochromocytoma. No gender restriction, between 16 and 75 years old.
You may qualify if:
- Age ≥ 16 years old and ≤ 75 years
- Patients diagnosed with adrenal associated diseases, including cushing syndrome, primary aldosteronism, primary hypoadrenalism, congenital adrenal hyperplasia and adrenal adenomas, incidentalomas, and carcinomas, pheochromocytoma, etc.
- Provide written informed consent
- Satisfactory compliance
You may not qualify if:
- Patients with significantly reduced life expectancy (less than 2 years)
- With Drug abuse
- With AIDS or syphilis or infectious diseases such as viral tuberculosis in active phase at enrollment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Endocrinology
Shanghai, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director, Head of Endocrinology, Principal Investigator, Clinical Professor
Study Record Dates
First Submitted
May 7, 2021
First Posted
May 18, 2021
Study Start
June 1, 2021
Primary Completion
April 30, 2026
Study Completion
April 30, 2026
Last Updated
February 14, 2022
Record last verified: 2022-01
Data Sharing
- IPD Sharing
- Will not share