Fact CheckerSign in

NCT07312149Not yet recruiting

Isolation of Pulmonary Veins Using the Box Technique in Patients Undergoing Sternotomy

BoxTer : Isolation of Pulmonary Veins Using the Box Technique in Patients Undergoing Sternotomy

Source: ClinicalTrials.gov · Last updated 24 Jun 2026

Brief summary (registry, in English)

Atrial Fibrillation (AF) is the most common cardiac arrhythmia worldwide, affecting approximately 2.8% of the population, with prevalence increasing with age. AF is associated with significant morbidity and mortality, accounting for about 25% of ischemic strokes, 10% of cryptogenic strokes, and a 10-40% annual increase in hospital admissions due to heart failure or anticoagulant-related events. About 10% of patients undergoing cardiac surgery have preoperative AF. In 1986, Dr. Cox introduced the MAZE procedure, a surgical technique to isolate AF triggers. Initially involving atrial incisions, it evolved to use radiofrequency lines, significantly reducing morbidity and mortality. The MAZE procedure is now strongly recommended (Class Ia evidence) for concomitant cardiac surgery. However, nearly 85% of eligible patients-especially those undergoing closed-chest cardiac surgery-do not receive this treatment due to technical challenges and limited reproducibility of the Cox-Maze IV technique. Pulmonary Vein Isolation (PVI) with posterior wall isolation (PWI-Box) has emerged as an effective alternative, offering similar outcomes to Cox-Maze IV with fewer adverse effects. Innovative devices like the GeminiS (Medtronic) enable minimally invasive, thoracoscopic PVI-PWI-Box procedures without opening the heart, even off-pump. This approach could expand the use of AF ablation during combined sternotomy surgeries, aligning with clinical guidelines. Primary Objective: Assess the efficacy of PWI-Box using GeminiS combined with other cardiac surgeries via sternotomy. Primary Endpoint: Recurrence rate of paroxysmal or persistent AF (per ESC definition) at 1 year postoperatively, confirmed by 24-hour Holter monitoring.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
16 Dec 2025
Start date
5 Oct 2026
Primary completion date
5 Oct 2030
Lead sponsor
Nantes University Hospital
NCT number
NCT07312149

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 5 Oct 2026 to the primary completion date, 5 Oct 2030
  • 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

  • Unplanned surgery (emergency)
  • Patients currently taking medication or using an experimental device that clinically interferes with the study's evaluation criteria and results.

Other illness

  • History of cardiac surgery (reoperation)

Other

  • Pregnant or breastfeeding women
  • Adults under guardianship, curatorship or judicial protection
  • Patients with a life expectancy of less than three years
  • Inability to comply with the monitoring schedule.
  • Contraindication to long-term anticoagulants

Who the study is looking for

  • Patients undergoing cardiac surgery via sternotomy
  • Concomitant use of the PWI box with GeminiS during surgery
  • Adult patients
  • Patients with the following characteristics: Preoperative paroxysmal/persistent/permanent AF; Duration of less than 5 years; And left atrium volume \<60 ml/m2
  • Informed patient who did not object to the collection of their data for the study

Age in the registry: 18 years to - · 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
CHU de Nantes
Coordinator of this site? Confirm its status
NantesFranceUnknown status

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