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Spanish Registry of Cryoballoon Ablation (RECABA)

Medtronic logo

Medtronic

Status

Completed

Conditions

Atrial Fibrillation

Treatments

Procedure: Balloon cryoablation

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

The purpose of this registry is to reflect on standard clinical practice in pulmonary vein cryoablation in Spanish hospitals, the different procedure protocols, details of intervention, complications, long-term follow-up strategy and results in these subjects.

Full description

With this study the investigators propose the performance of a prospective registry of pulmonary vein cryoablation in subjects with paroxysmal or persistent AF at Spanish sites to estimate evaluate the efficacy of the cryoablation procedure at 12 months, defined as the absence of recurrences of atrial fibrillation.

Secondary objectives are also defined as:

  • Description of the profile of subjects who undergo this type of procedure (demographic factors, cardiovascular risk factors, medication, physical activity, sleep apnea, alcohol, smoking, chronic pulmonary disease, obesity, etc.).
  • To evaluate the acute efficacy of the procedure: complete isolation of the pulmonary veins demonstrated by the successful electrical disconnection of the pulmonary veins in the cryoablation procedure.
  • Description of the complications related to the procedure.
  • To evaluate the use of healthcare resources which this cryoablation procedure entails.

Enrollment

1,742 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signature of the Data Release Form
  • Subjects ≥ 18 years old
  • Subjects who meet the indication for the Cryoballoon Ablation procedure.

Exclusion criteria

  • Subjects with a life expectancy of less than 12 months.
  • Subjects who meet the exclusion criteria defined by local legislation (e.g., age, pregnancy, breastfeeding, etc.).
  • Subjects who may currently be enrolled, or who plan to take part, in a study with a drug or device that may cause bias during the course of this study.
  • Co-participation in concurrent trials is only allowed when documented pre-approval is obtained from the Medtronic study manager.

Trial design

Trial documents
2

Trial contacts and locations

28

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Data sourced from clinicaltrials.gov

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