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
- Diseases
- Atrial fibrillation
- 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
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU de Nantes Coordinator of this site? Confirm its status | Nantes | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.