Clinical trial Recruiting at 1 site Observational Ages 3 to 80

Understanding cardiac tumors and their risks

Official title: Characteristics of Cardiac Tumor and the Risk Stratification of Subsequent Adverse Events (UNIQUE): an Investigator-initiated, National, Multicenter, Retrospective-prospective, Cohort Study

Run by First Affiliated Hospital Xi'an Jiaotong University · NCT06100328 · Data updated 2026-11-12

This study is trying to gather information from patients with heart tumors to better understand their risks and develop a way to predict how these tumors might behave over time.

Quick facts

Study typeObservational
Ages3 Years to 80 Years
SexAll
Enrollment40 (estimated)
SponsorFirst Affiliated Hospital Xi'an Jiaotong University
Academic / other
Locations1 site (Xi'an, Shaanxi)
StatusRecruiting
StartedOctober 26, 2023
Main results expectedJuly 31, 2030
Study endsJuly 31, 2030
Registry record updatedJuly 12, 2024
Trial IDNCT06100328 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients diagnosed with various types of cardiac tumors who are regularly followed up at a cardiovascular center.

Probably not a fit

Patients under 3 years or over 80 years old, pregnant or lactating women, and those unable to provide informed consent will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to collect and analyze clinical and biological data from patients diagnosed with cardiac tumors, both retrospectively and prospectively. It will utilize various techniques, including molecular biology and multi-omics analysis, to develop a prognostic model for these tumors. The research will involve a long-term follow-up cohort and management system, assessing disease characteristics, progression patterns, and long-term prognosis. Data will be gathered from cases spanning from 2003 to 2030, creating a comprehensive understanding of cardiac tumors.

Why it matters

Potential benefit: If successful, this study could improve risk stratification and management of patients with cardiac tumors.

How similar studies have gone: While there have been studies on cardiac tumors, this approach of combining retrospective and prospective data collection with multi-omics analysis is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients who are regularly visited and followed up in the corresponding cardiovascular center.
* All patients must meet at least one of the following diagnostic criteria for cardiac neoplasms: 1. Cardiac myxoma group; 2. Cardiac fibroma group; 3. Cardiac lipoma group; 4. Cardiac hemangioma group; 5. Cardiac undifferentiated sarcoma; 6. Cardiac angiosarcoma group; 7. Cardiac rhabdomyosarcoma group; 8. Cardiac lymphoma group; 9. Cardiac metastasis group; 10. Other cardiac tumors group.

Exclusion Criteria:

* Age \<3 years or \>80 years old.
* Pregnant and lactating women.
* The patient declined to provide informed consent to participate in the study.
* None of the above was met, but the patient was temporarily unable to sign the informed consent form due to coma and other reasons, and no legal representative signed it instead. Depending on the patient's condition, the patient may not be able to regain consciousness and sign the informed consent form.

Where it's running

  • First Affiliated Hospital of Xi'an Jiantong University
    Xi'an, Shaanxi, China
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.