Clinical trial · Interventional
The Safety and Efficacy Evaluation of Echocardiography-guided Percutaneous Radiofrequency Ablation for Cardiac Tumors: a Single-arm, Prospective, Single-center Clinical Study
NCT06830512CI-TRIAL-00086070recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The safety and efficacy evaluation of echocardiography-guided percutaneous radiofrequency ablation (Liwen prcocedure) for cardiac tumors: a single-arm, prospective, single-center clinical study.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Heart Neoplasms | Heart Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Echocardiography-guided percutaneous radiofrequency ablation for cardiac tumors | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- treatment group
- description
- Echocardiography-guided percutaneous radiofrequency ablation
- interventionNames
- Procedure: Echocardiography-guided percutaneous radiofrequency ablation for cardiac tumors
Primary outcomes (2)
- measure
- Effective response rate (Effective defined as ≥30% reduction in the total longest diameter of the target lesion first detected during the postoperative follow-up period and confirmed 4 weeks after surgery)
- timeFrame
- 1 year
- measure
- 30 days after surgery: Cardiovascular mortality
- timeFrame
- 1 year
Secondary outcomes (5)
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: 1. 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; 2. Patients who cannot be completely excised by surgery, cannot tolerate surgery or refuse surgery; 3. 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. Exclusion Criteria: 1. Previously documented persistent ventricular tachycardia or ventricular fibrillation, supraventricular tachycardia with hemodynamic disturbance, cardiac arrest, and high atrioventricular block; 2. Previous history of tumor or thromboembolism exfoliating organ embolism; 3. Combined with other heart diseases requiring surgical treatment; 4. Active infections should be treated with antibiotics; 5. Bleeding constitution and coagulation disorders, or anticoagulation, antiplatelet therapy contraindications; 6. Patients who are pregnant, breastfeeding or planning to become pregnant during the clinical study; 7. The disease will cause difficulties in the evaluation of treatment, such as mental illness, metabolic disease, etc.; 8. Patients who cannot tolerate general anesthesia; 9. Severe liver, kidney, lung, brain and other major organ failure; 10. There are no patients who are suitable for the injection path of Liwen operation; 11. Other diseases deemed unsuitable for inclusion by the researchers; 12. The researcher judged that the patients' dependence was poor and could not complete the study.
References
Publications (0)
Data not yet available
No reference posted for this study.