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Consistency of LGE-MRI Fibrosis and EAM Low-voltage Area

N

National Center for Cardiovascular Diseases

Status

Enrolling

Conditions

Atrial Fibrillation

Treatments

Diagnostic Test: LGE-MRI Scan

Study type

Observational

Funder types

Other

Identifiers

NCT06552845
2023-2223

Details and patient eligibility

About

This study aims to:

  1. Assess the consistency of LGE-MRI bi-atrial fibrosis and electroanatomical mapping of bi-atrial low voltage region
  2. To evaluate the electroanatomical characteristics of different types of fibrosis (dense fibrosis, patchy fibrosis, etc.) in different locations of the left and right atrium;
  3. To explore the correlation between preoperative and postoperative bi-atrial fibrosis and long-term recurrence in patients with atrial fibrillation.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Adult patients (≥18 years old) who are willing to participate in this study and can sign informed consent;
  2. Atrial fibrillation was diagnosed and catheter ablation was proposed

Exclusion criteria

  1. Left atrial thrombus or left atrial appendage thrombus;
  2. Severe chronic obstructive pulmonary disease (FEV1/ FVC<70%, FEV1<50% predicted value);
  3. Absolute contraindications of anticoagulation therapy;
  4. Currently pregnant;
  5. Contraindications for LGE-MRI (claustrophobia, pacemaker implantation, eGFR<30ml/min for renal insufficiency, severe obesity, pregnancy, gadolinium chelating agent allergy, etc.);
  6. refuse to participate in the study;
  7. other physical or mental incapacity to participate in the study.

Trial design

50 participants in 1 patient group

Observational Group
Description:
Inclusion Criteria 1. Adult patients (≥18 years old) who are willing to participate in this study and can sign informed consent; 2. Atrial fibrillation was diagnosed and catheter ablation was proposed Exclusion criteria a) Left atrial thrombus or left atrial appendage thrombus; b) Severe chronic obstructive pulmonary disease (FEV1/ FVC\<70%, FEV1\<50% predicted value); c) Absolute contraindications of anticoagulation therapy; d) Currently pregnant; e) Contraindications for LGE-MRI (claustrophobia, pacemaker implantation, eGFR\<30ml/min for renal insufficiency, severe obesity, pregnancy, gadolinium chelating agent allergy, etc.); f) refuse to participate in the study; g) other physical or mental incapacity to participate in the study.
Treatment:
Diagnostic Test: LGE-MRI Scan

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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