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NCT06830512Recruiting

The Safety and Efficacy Evaluation of Echocardiography-guided Percutaneous Radiofrequency Ablation for Cardiac Tumors: a Single-arm, Prospective, Single-center Clinical Study

Source: ClinicalTrials.gov · Last updated 17 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The safety and efficacy evaluation of echocardiography-guided percutaneous radiofrequency ablation (Liwen prcocedure) for cardiac tumors: a single-arm, prospective, single-center clinical study.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
7 Jan 2025
Start date
24 Jan 2024
Primary completion date
30 Dec 2025
Lead sponsor
Xijing Hospital
NCT number
NCT06830512

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 24 Jan 2024 to the primary completion date, 30 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously documented persistent ventricular tachycardia or ventricular fibrillation, supraventricular tachycardia with hemodynamic disturbance, cardiac arrest, and high atrioventricular block;
  • Previous history of tumor or thromboembolism exfoliating organ embolism;
  • Active infections should be treated with antibiotics;

Other illness

  • Combined with other heart diseases requiring surgical treatment;
  • Bleeding constitution and coagulation disorders, or anticoagulation, antiplatelet therapy contraindications;
  • The disease will cause difficulties in the evaluation of treatment, such as mental illness, metabolic disease, etc.;
  • Severe liver, kidney, lung, brain and other major organ failure;
  • Other diseases deemed unsuitable for inclusion by the researchers;

Other

  • Patients who are pregnant, breastfeeding or planning to become pregnant during the clinical study;
  • Patients who cannot tolerate general anesthesia;
  • There are no patients who are suitable for the injection path of Liwen operation;
  • The researcher judged that the patients' dependence was poor and could not complete the study.

Who the study is looking for

  • Hemodynamic changes caused by cardiac tumors or patients with obvious clinical symptoms such as chest tightness, shortness of breath, palpitations, etc., or the risk of embolization of intracardial tumors;
  • Patients who cannot be completely excised by surgery, cannot tolerate surgery or refuse surgery;
  • The patient was informed of the nature of the clinical study and agreed to participate in all the requirements of the clinical study, signed the informed consent, and agreed to complete the follow-up and follow-up examination required.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Xijing hospital
Coordinator of this site? Confirm its status
Xi'anChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.