Cardiovascular Outcomes and Risk Evaluation Among Recipients of Hematopoietic Stem Cell Transplantation
CORE-HCT
1 other identifier
observational
10,000
1 country
16
Brief Summary
This is a prospective, multicenter observational study for recipients of hematopoietic stem cell transplantation. Patients who underwent hematopoietic stem cell transplantation at the participating centers will be entrolled in the study. The clinical characteristics, laboratory profiles, management measures, and clinical outcomes such as post-transplant cardiovascular events will be prospectively collected.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2026
Longer than P75 for all trials
16 active sites
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
Study Start
First participant enrolled
January 1, 2026
CompletedFirst Submitted
Initial submission to the registry
January 9, 2026
CompletedFirst Posted
Study publicly available on registry
January 16, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2036
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2036
January 16, 2026
January 1, 2026
10.5 years
January 9, 2026
January 9, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Major adverse cardiovascular events (MACE)
Major adverse cardiovascular events (MACE) after hematopoietic stem cell transplantation.
At 30 days, 100 days, 3 months, 6 months, 1 years, 3 years, 5 years post hematopoietic stem cell transplantation.
Secondary Outcomes (4)
Cardiovascular events
At 30 days, 100 days, 3 months, 6 months, 1 years, 3 years, 5 years post hematopoietic stem cell transplantation.
Overall survival
At 30 days, 100 days, 3 months, 6 months, 1 years, 3 years, 5 years post hematopoietic stem cell transplantation.
Event-free survival
At 30 days, 100 days, 3 months, 6 months, 1 years, 3 years, 5 years post hematopoietic stem cell transplantation.
Complications of hematopoietic stem cell transplantation
At 30 days, 100 days, 3 months, 6 months, 1 years, 3 years, 5 years post hematopoietic stem cell transplantation.
Study Arms (1)
Patients undergoing hematopoietic stem cell transplantation
Patients who undergo allogeneic hematopoietic stem cell transplantation at participating medical center.
Eligibility Criteria
Patients who undergo hematopoietic cell transplantation at any of the participating medical centers.
You may qualify if:
- Patients who undergo hematopoietic cell transplantation at any of the participating medical centers.
You may not qualify if:
- Any other conditions that, in the opinion of the investigator, can interfere with the interpretation of data.
- Patient request to withdraw from the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Peking University People's Hospitallead
- First Affiliated Hospital of Zhejiang Universitycollaborator
- Union Hospital, Tongji Medical College, Huazhong University of Science and Technologycollaborator
- Tongji Hospital, Affiliated to Tongji Medical College of Huazhong University of Science and Technologycollaborator
- Xinqiao hospital of the third military medical universitycollaborator
- The First Affiliated Hospital of Zhengzhou Universitycollaborator
- Sun Yat-Sen University Cancer Centercollaborator
- Sichuan Provincial People's Hospitalcollaborator
- First Affiliated Hospital of Harbin Medical Universitycollaborator
- First Affiliated Hospital Xi'an Jiaotong Universitycollaborator
- First Affiliated Hospital of Xinjiang Medical Universitycollaborator
- Chinese PLA General Hospitalcollaborator
- Peking University Shenzhen Hospitalcollaborator
- Peking University Third Hospitalcollaborator
- Peking University First Hospitalcollaborator
- Hematology Hospital of Chinese Academy of Medical Sciences (Hematology Research Center of Chinese Academy of Medical Sciences)collaborator
Study Sites (16)
Chinese PLA General Hospital
Beijing, Beijing Municipality, China
Peking University First Hospital
Beijing, Beijing Municipality, China
Peking University People's Hospital
Beijing, Beijing Municipality, China
Peking University Third Hospital
Beijing, Beijing Municipality, China
Xinqiao hospital of the third military medical university
Chongqing, Chongqing Municipality, China
Sun Yat-sen University Cancer Center, Sun Yat-sen University
Guangzhou, Guangdong, China
Peking University Shenzhen Hospital
Shenzhen, Guangdong, China
First Affiliated Hospital of Harbin Medical University
Harbin, Heilongjiang, China
The First Affiliated Hospital of Zhengzhou University
Zhengzhou, Henan, China
Tongji Hospital, Affiliated to Tongji Medical College of Huazhong University of Science and Technology
Wuhan, Hubei, China
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, China
First Affiliated Hospital Xi'an Jiaotong University
Xi'an, Shaanxi, China
Sichuan Provincial People's Hospital
Chengdu, Sichuan, China
Hematology Hospital of Chinese Academy of Medical Sciences (Hematology Research Center of Chinese Academy of Medical Sciences)
Tianjin, Tianjin Municipality, China
First Affiliated Hospital of Xinjiang Medical University
Ürümqi, Xinjiang, China
First Affiliated Hospital of Zhejiang University
Hangzhou, Zhejiang, China
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 5 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
January 9, 2026
First Posted
January 16, 2026
Study Start
January 1, 2026
Primary Completion (Estimated)
June 30, 2036
Study Completion (Estimated)
December 31, 2036
Last Updated
January 16, 2026
Record last verified: 2026-01