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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04529629
Other study ID # CCEMD-2020-0825
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 30, 2021
Est. completion date August 30, 2041

Study information

Verified date December 2021
Source Shanghai Jiao Tong University School of Medicine
Contact Yiran Jiang, MD
Phone 8621-64370045
Email rainy0409@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The adrenal gland is an important organ that produces life hormones. There are many types of adrenal tumors, which tend to occur in young adults and affect the whole body. It has the dual threat: hormone secretion and tumor metastasis. At present, there are four major dilemmas in the clinical diagnosis and treatment of adrenal tumors: 1) Pulse secretion of the hormones, which are affected by many factors; and the diagnostic value of single hormone is limited; 2) Traditional imaging cannot accurately reflect the characteristics of hormone secretion. The prognosis cannot be accurately predicted; 3) The molecular characteristics of tumor cells and the microenvironment are unclear, making it difficult to implement early diagnosis and precise treatment; 4) Traditional pathology cannot determine the nature and long-term prognosis of the tumor, which makes the treatment delay, and the disease prognosis is extremely poor. It threatens the lives of patients. Starting from solving the above-mentioned key problems in the early stage, the research team has systematically established new clinical diagnostic technologies, hormone dynamic tests to accurately assess hormone secretion and segmented blood collection hormone determination technologies to accurately locate adrenal tumors; A series of important research results have been published in Science, Lancet Diabetes & Endocrinology, Cell Research, etc To sum up, the goal of this research is improving the early diagnosis rate of complicated adrenal tumors especially in malignant tumors, developing the optimal treatment plan, avoiding unnecessary surgical treatment, improving the quality of life of patients, reducing mortality. This project will further integrate the adrenal cortex and medulla hormone mass spectrometry detection and the molecular markers of adrenal tumors through phenotypic, functional imaging, and molecular pathological evaluations, and built a sensitive drug screening platform that integrates visual drug response and molecular characteristics, thereby achieving precise diagnosis and treatment of complicated adrenal tumors.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date August 30, 2041
Est. primary completion date August 30, 2040
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Age = 18 years old and = 75 years - Diagnosis of Patients with primary aldosteronism, pheochromocytoma, and cortical cancer - Gender: males and females - Provide written informed consent - Satisfactory compliance Exclusion Criteria: 1. Patients with renal insufficiency (Cr>2 times the upper limit of normal). 2. Patients with a history of liver cirrhosis. 3. Patients who are currently using corticosteroids. 4. Patients with cardiac insufficiency (NYHA cardiac function classification grade 3 and above or EF<50%). 5. Patients with stroke and acute myocardial infarction in the past 6 months. 6. Patients during pregnancy and lactation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
surgery or drug
pheochromocytoma and adrenocortical carcinoma need surgery and primary aldosteronism need drug according to the genetic results

Locations

Country Name City State
China Ruijin Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Jiao Tong University School of Medicine

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary tumor biochemical marker treatment response Complete remission (normalization of tumor markers);
Partial remission (reduction of tumor markers = 50%); ?No change (decrease of tumor markers <50% or increase =25%); ?Disease progression (tumor markers increased> 25%).
20 years
Primary Tumor volume assessment: According to RECIST (version 1.1). Complete response: All target lesions disappear, and the short axis of any pathological lymph nodes must be reduced to <10 mm.
Partial Response: The total diameter of the target lesions is reduced by at least 30% compared with the baseline.
Progressive Disease: Take the minimum value of the sum of the diameters of all target lesions measured during the study as the reference, and the relative increase in diameter sum by at least 20% ?Stable Disease: Based on the minimum value of the sum of the diameters of all target lesions measured during the study, the reduction of the target lesion did not reach PR, and the degree of increase did not reach PD, between PR and PD.
20 years