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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06386445
Other study ID # XJTU1AF-CRF-2023-XK013
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 1, 2024
Est. completion date December 31, 2026

Study information

Verified date April 2024
Source First Affiliated Hospital Xi'an Jiaotong University
Contact xiaonig wang, M.D.
Phone 02985323473
Email wangxn99@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to establish a cohort of 500 patients with hematological disease who undergoing allogeneic hematopoietic stem cell transplantation in the northwest region. All patients will be followed up at the outpatient clinic once a week after transplantation until 100 days after transplantation to observe the presence of acute graft versus host disease, acute kidney damage, and major cardiovascular adverse events. Serum samples from the day before pre-treatment, day after pre-treatment, 2 weeks,4 weeks,8 weeks and 12 weeks after transplantation will be detected by metabolomics sequencing.The primary objective is to explore the serum metabolic markers of acute graft versus host disease,acute kidney injury, and major adverse cardiac events within 100 days after transplantation,the secondary objective is to observe the high-risk factors for early complications.


Description:

This study aims to establish a cohort of 500 patients with hematological disease who undergoing allogeneic hematopoietic stem cell transplantation in the northwest region. All patients will be followed up at the outpatient clinic once a week after transplantation until 100 days after transplantation to observe the presence of acute graft versus host disease, acute kidney damage, and major cardiovascular adverse events. Baseline characterisitcs of patients, including gender, age, disease type, transplant type, donor gender and age, pre-transplant baseline electrocardiogram, myocardial enzymology, renal function, and other indicators were recorded. Serum samples from the day before pre-treatment, day after pre-treatment, 2 weeks,4 weeks,8 weeks and 12 weeks after transplantation will be detected by metabolomics sequencing.The primary objective is to explore the serum metabolic markers of acute graft versus host disease,acute kidney injury, and major adverse cardiac events within 100 days after transplantation,the secondary objective is to observe the high-risk factors for early complications.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 500
Est. completion date December 31, 2026
Est. primary completion date December 31, 2026
Accepts healthy volunteers
Gender All
Age group 0 Years to 65 Years
Eligibility Inclusion Criteria: - Age = 65 years old; Gender unlimited; Normal heart and kidney function before transplantation; Patients with indications for allogeneic hematopoietic stem cell transplantation. Exclusion Criteria: - CREA or BUN higher than the normal upper limit value before transplantation; Individuals with a history of arrhythmia, heart failure, or PCI stent implantation prior to transplantation; Patients with mental illness; Those who are unwilling to sign informed consent.

Study Design


Intervention

Other:
Serum metabolomics sequencing
Serum samples from the day before pre-treatment, day after pre-treatment, 2 weeks,4 weeks,8 weeks and 12 weeks after transplantation will be detected by metabolomics sequencing.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
First Affiliated Hospital Xi'an Jiaotong University

Outcome

Type Measure Description Time frame Safety issue
Primary acute graft versus host disease skin,liver and gastrointestinal acute graft versus host disease within 100 days after transplantation
Secondary acute kidney injury Included AKI-R, AKI-I, and AKI-F ,the criteria for classification of AKI-R, AKI-I, and AKI-F are as follows: AKI-R was considered if there was an increase in serum creatinine to more than 1.5-fold of baseline value or a urinary output lower than 0.5 ml/kg/h for 6 h. AKI-I was considered if there was an increase in serum creatinine to more than 2-fold of baseline value or urinary output lower than 0.5 ml/kg/h for 12 h. AKI-F was considered if there was an increase in serum creatinine to more than 3-fold baseline value or urinary output lower than 0.3 ml/kg/h for 24 h. within 100 days after transplantation
Secondary major adverse cardiac events cardiovascular mortality, coronary events, heart failure, atrial fibrillation/flutter within 100 days after transplantation
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