Quick Yielding Modified Short-Distance Fenestration Technique for the Treatment of Complex Aortic Arch Diseases: a Multicenter Single-Arm Objective Performance Criteria Trial(QYM-Tech Study)

Not Applicable

Active, not recruiting

• Conditions: Thoracic Aortic Dissection; Thoracic Aortic Aneurysm (true Aneurysm); Thoracic Pseudoaneurysm; Penetrating Aortic Ulcer; Intramural Hematoma of the Thoracic Aorta

• Registration Number: NCT06639243
• Lead Sponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

Brief Summary

Background: This study investigates the safety and efficacy of a novel surgical approach combining thoracic endovascular aortic repair (TEVAR) and in situ fenestration reconstruction of supra-aortic branches using the Quick Yielding Modified (QYM) technique. This procedure aims to address complex aortic arch diseases, providing an alternative to more invasive open surgical interventions.

Methods: This is a prospective, multicenter, single-arm, interventional study involving 87 patients across 3 centers. Eligible participants are adults aged 18-80 diagnosed with thoracic aortic dissection, thoracic aortic aneurysm (true or pseudo), penetrating aortic ulcer, or intramural hematoma, necessitating supra-aortic branch vessel reconstruction. The surgical protocol involves TEVAR combined with the QYM technique for fenestration and revascularization.

Primary Outcome: The primary endpoint is the incidence of major adverse events (MAE) within 30 days post-operation.

Secondary Outcomes: Secondary endpoints include 12-month aortic treatment success, all-cause mortality, aortic-related mortality, incidence of severe adverse events, occurrence of Type I/III endoleaks, stent graft migration, patency of revascularized branches, and rates of conversion to open surgery or reintervention due to aortic complications.

Inclusion/Exclusion Criteria: Key inclusion criteria include imaging-confirmed thoracic aortic disease requiring endovascular repair with a proximal landing zone in the aortic arch (Zone 0) and suitable anatomical features for stent placement. Patients with recent systemic infections, severe coronary artery involvement, or other significant comorbidities were excluded.

Follow-up and Statistical Analysis: Patients will undergo follow-ups at discharge, 30 days, 6 months, and 12 months post-surgery. Statistical analyses will include descriptive statistics of quantitative and categorical variables, with statistical significance set at a one-sided p-value \< 0.025.

This study aims to provide critical insights into the clinical applicability of the QYM technique, potentially broadening therapeutic options for complex aortic arch diseases.

Detailed Description

Not available

Study Timeline

• Study Start: 2024-01-01
• Status Verified: 2024-10
• Study First Submitted: 2024-10-10
• Study First Submitted QC: 2024-10-10
• Last Update Submitted: 2024-10-10
• Study First Posted: 2024-10-14
• Last Update Posted: 2024-10-14
• Primary Completion: 2028-12-31
• Study Completion: 2028-12-31

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 87

Inclusion Criteria

1. Age: Patients between 18 and 80 years of age.

2. Diagnosis: Patients with the following thoracic aortic conditions confirmed by imaging (CTA):

   • Thoracic aortic dissection
   • True thoracic aortic aneurysm
   • Thoracic pseudoaneurysm
   • Penetrating aortic ulcer
   • Intramural hematoma

3. Indication for Treatment: Patients requiring supra-aortic branch vessel reconstruction due to rupture, impending rupture, malperfusion syndrome, rapid expansion, uncontrolled pain, aneurysmal dilation, or for prophylactic reasons.

4. Proximal Landing Zone: Patients whose proximal stent landing zone is in Zone 0 of the aortic arch.

5. Aortic Anatomy:

   • Length of ascending aorta >4 cm (from the sinotubular junction to the proximal edge of the brachiocephalic artery).
   • Diameter of ascending aorta between 24 mm and 44 mm.

6. Access Vessel Anatomy:

   • Iliac artery diameter ≥7 mm.
   • Brachiocephalic artery diameter ≤24 mm, and length ≥20 mm.

7. Informed Consent: Patients who have been informed about the nature of the study and agreed to participate by signing the informed consent form.

Exclusion Criteria

1. Infection: Patients with systemic infections within the last 3 months.

2. Recent Neck Surgery: Patients who underwent neck surgery within the past 3 months.

3. Coronary Involvement: Patients with disease extending to the coronary arteries or aortic valve.

4. Infectious or Autoimmune Diseases: Patients with conditions such as infectious aortic disease, large vessel vasculitis, or Marfan syndrome (or other connective tissue disorders).

5. Severe Vascular Conditions: Patients with severe stenosis, calcification, thrombosis, or tortuosity of the carotid or subclavian arteries.

6. Heart Transplant: Patients who have undergone heart transplantation.

7. Recent Cardiac Events: Patients who had a myocardial infarction or stroke within the last 3 months.

8. Advanced Heart Failure: Patients with New York Heart Association (NYHA) Class IV heart failure.

9. Active Gastrointestinal Conditions: Patients with active peptic ulcer disease or upper gastrointestinal bleeding within the past 3 months.

10. Hematologic Abnormalities:

    • Leukopenia (white blood cell count < 3×10⁹/L)
    • Acute anemia (hemoglobin < 90 g/L)
    • Thrombocytopenia (platelet count < 50×10⁹/L)
    • History of bleeding disorders or coagulopathy.

11. Renal Function: Patients with impaired renal function (creatinine > 265 µmol/L) or those with end-stage renal disease.

12. Pregnancy or Lactation: Pregnant or breastfeeding women.

13. Allergy to Contrast Media: Patients with an allergy to the contrast agents used in imaging.

14. Life Expectancy: Patients with an expected survival of less than 12 months.

15. Concurrent Research Participation: Patients involved in other drug or device trials.

16. Other Medical Conditions: Any other disease or condition that, in the opinion of the investigator, may interfere with the endovascular treatment or the patient's ability to participate in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Incidence of Major Adverse Events (MAE) Within 30 Days Post-Operation	30 days post-operation	This primary outcome measure evaluates the safety of the Quick Yielding Modified (QYM) technique by assessing the incidence of major adverse events (MAE) occurring within 30 days following the surgical intervention. Major adverse events include any significant complications that could impact patient health and recovery, such as stroke, myocardial infarction, aortic rupture, organ failure, or death. The goal is to determine the short-term safety profile of the intervention, providing critical information on its clinical viability for patients with complex aortic arch diseases. Data will be collected through patient monitoring, clinical assessments, and medical records during the specified follow-up period.

Secondary Outcome Measures

Name	Time	Method
Aortic Treatment Success Rate at 12 Months	Up to 12 months post-operation	This secondary outcome measure assesses the effectiveness of the Quick Yielding Modified (QYM) technique by evaluating the rate of successful treatment of the aortic condition at 12 months post-intervention. Treatment success is defined as the absence of significant complications, such as re-intervention or aortic-related adverse events, and the proper functioning of the thoracic stent graft with no significant endoleaks. This measure provides insight into the long-term effectiveness and durability of the surgical intervention.
All-Cause Mortality	Up to 12 months post-operation	This secondary outcome measure records the rate of all-cause mortality among participants within the study period, allowing for an evaluation of overall patient survival following the intervention. It provides crucial data on the safety and effectiveness of the QYM technique in comparison to the underlying risk of mortality associated with complex aortic arch diseases.
Aortic-Related Mortality	Up to 12 months post-operation	This secondary outcome measure focuses specifically on mortality directly related to aortic conditions or complications arising from the surgical intervention. This measure helps to evaluate the long-term safety of the QYM technique concerning life-threatening aortic issues.
Incidence of Severe Adverse Events	Up to 12 months post-operation	This measure tracks the occurrence of severe adverse events in participants, including complications such as stroke, myocardial infarction, and organ failure that are serious enough to require medical intervention. Monitoring these events provides a broader understanding of the risks associated with the procedure.
Occurrence of Type I or III Endoleaks	Up to 12 months post-operation	This measure evaluates the incidence of Type I or Type III endoleaks following the intervention. Endoleaks are complications that can lead to re-intervention, and monitoring them is critical for assessing the effectiveness of the stent graft placement.
Rate of Stent Graft Migration	Up to 12 months post-operation	This measure assesses the migration of the thoracic stent graft from its original position within the aorta. Stent migration can affect the success of the procedure and requires careful monitoring to ensure the stent remains securely in place.
Patency Rate of Revascularized Branch Vessels	Up to 12 months post-operation	This measure evaluates the patency (openness and functionality) of the revascularized supra-aortic branches at follow-up visits. A high patency rate indicates successful reconstruction and blood flow restoration to these vessels.
Rate of Conversion to Open Surgery or Reintervention Due to Aortic Complications	Up to 12 months post-operation	This measure tracks the incidence of participants who require conversion to open surgery or additional interventions due to complications related to the aorta after the initial procedure. It provides insight into the long-term risks and effectiveness of the QYM technique.
Incidence of Major Adverse Events (MAE) at 12 Months	12 months post-operation	This measure assesses the occurrence of major adverse events (MAE) within the 12-month follow-up period. Major adverse events include complications such as stroke, myocardial infarction, aortic rupture, or death. Monitoring the incidence of these events over the long term provides additional data on the safety and durability of the Quick Yielding Modified (QYM) technique.
Freedom from Aortic Rupture	12 months post-operation	This outcome tracks the percentage of participants who remain free from aortic rupture following the QYM technique over the course of 12 months. Aortic rupture is a life-threatening event, and the goal is to assess whether the intervention effectively prevents this complication in patients with complex aortic arch diseases.
Freedom from Reintervention	12 months post-operation	This measure evaluates the percentage of participants who do not require additional surgical or endovascular interventions on the thoracic aorta or supra-aortic branches after the initial procedure. The goal is to assess the long-term effectiveness of the QYM technique and its ability to prevent the need for further treatments.

Trial Locations

Locations (1)

Department of Vascular Surgery, General Surgery Clinical Center, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.; 🇨🇳 Shanghai, Shanghai, China