NCT04890444

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

57
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2021

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
11 days until next milestone

First Posted

Study publicly available on registry

May 18, 2021

Completed
14 days until next milestone

Study Start

First participant enrolled

June 1, 2021

Completed
4.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
Last Updated

February 14, 2022

Status Verified

January 1, 2022

Enrollment Period

4.9 years

First QC Date

May 7, 2021

Last Update Submit

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

Age16 Years - 75 Years
Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

Cushing SyndromeHyperaldosteronismAdrenal InsufficiencyAdrenal Hyperplasia, CongenitalACTH Syndrome, EctopicAdrenal incidentalomaAdrenal Cortex NeoplasmsPheochromocytoma

Condition Hierarchy (Ancestors)

Adrenocortical HyperfunctionAdrenal Gland DiseasesEndocrine System DiseasesAdrenogenital SyndromeDisorders of Sex DevelopmentUrogenital AbnormalitiesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesGenetic Diseases, InbornSteroid Metabolism, Inborn ErrorsMetabolism, Inborn ErrorsMetabolic DiseasesNutritional and Metabolic DiseasesGonadal DisordersParaneoplastic Endocrine SyndromesParaneoplastic SyndromesNeoplasmsAdrenal Gland NeoplasmsEndocrine Gland NeoplasmsNeoplasms by SiteAdrenal Cortex DiseasesParagangliomaNeuroendocrine TumorsNeuroectodermal TumorsNeoplasms, Germ Cell and EmbryonalNeoplasms by Histologic TypeNeoplasms, Nerve Tissue

Central Study Contacts

shouyue SUN, MD

CONTACT

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

Locations