Pilot study of New Generation Arrhythmia Treatment
- Conditions
- atrial fibrillationD001281
- Registration Number
- JPRN-jRCTs032210505
- Lead Sponsor
- Wakatsuki Masaru
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 3
(1) Written consent for participation in this study has been obtained from the subject or a surrogate at the time consent is obtained.
(2) 18 years of age or older
3) The following patients with confirmed atrial fibrillation
i) Cancer patients
ii) Patients who are drug-refractory and eligible for catheter ablation, but difficult to perform because of the following reasons Patients who are physically too weak to undergo catheter ablation (PS1-3), have low ADL (Barthel Index 41-85), or are allergic to anesthesia.
1) Patients with a life expectancy of more than 12 months due to other diseases such as malignant tumors, or patients with poor general health (PS 4, or Barthel Index score of 40 or less)
2) Heart failure dependent on inotropic drugs or left ventricular assist device
3) Patients with organic heart disease requiring surgical treatment
4) Requires inpatient treatment for acute coronary syndrome or acute heart failure
5) High risk of radiation pneumonitis, such as idiopathic pulmonary fibrosis (IPF) evident on chest CT
(6) Undergoing maintenance hemodialysis or peritoneal dialysis
(7) The principal investigator judges that participation in this study is inappropriate due to reasons such as pregnancy or other illnesses that make it difficult to conduct necessary examinations or follow-up studies.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method