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)
Key facts
- Who runs it
- Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
- Where
- China1 site in 1 countryChoose a country to see its sites
- Trial code
- Status
- Active, not recruiting
- People taking part
- 87 people, planned
- Started
- 1 Jan 2024
- Expected to end
- 31 Dec 2028
- Type of study
- Interventional
- Treatments tested
- QYM Technique
- Record updated
- 13 November 2026
Who can take part
- Age
- 18 years to 80 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 23 criteriaShow less
Who can take part
- Age: Patients between 18 and 80 years of age
- 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
- 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
- Proximal Landing Zone: Patients whose proximal stent landing zone is in Zone 0 of the aortic arch
- 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
- Access Vessel Anatomy:; Iliac artery diameter ≥7 mm; Brachiocephalic artery diameter ≤24 mm, and length ≥20 mm
- Informed Consent: Patients who have been informed about the nature of the study and agreed to participate by signing the informed consent form
Who cannot take part
- Recent Neck Surgery: Patients who underwent neck surgery within the past 3 months
- Concurrent Research Participation: Patients involved in other drug or device trials
- Infection: Patients with systemic infections within the last 3 months
- Coronary Involvement: Patients with disease extending to the coronary arteries or aortic valve
- Infectious or Autoimmune Diseases: Patients with conditions such as infectious aortic disease, large vessel vasculitis, or Marfan syndrome (or other connective tissue disorders)
- Severe Vascular Conditions: Patients with severe stenosis, calcification, thrombosis, or tortuosity of the carotid or subclavian arteries
- Heart Transplant: Patients who have undergone heart transplantation
- Recent Cardiac Events: Patients who had a myocardial infarction or stroke within the last 3 months
- Advanced Heart Failure: Patients with New York Heart Association (NYHA) Class IV heart failure
- Active Gastrointestinal Conditions: Patients with active peptic ulcer disease or upper gastrointestinal bleeding within the past 3 months
- Allergy to Contrast Media: Patients with an allergy to the contrast agents used in imaging
- 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
- 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
- Renal Function: Patients with impaired renal function (creatinine \> 265 µmol/L) or those with end-stage renal disease
- Pregnancy or Lactation: Pregnant or breastfeeding women
- Life Expectancy: Patients with an expected survival of less than 12 months
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
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.
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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.
The group in the trial
- QTM Technique Treatment ArmTreatment being tested
In this study, all participants will undergo the Quick Yielding Modified (QYM) technique, which combines thoracic endovascular aortic repair (TEVAR) with in situ fenestration and revascularization of the supra-aortic branches. This technique is designed to treat patients with complex aortic arch diseases, including thoracic aortic dissection, true and pseudoaneurysms, penetrating aortic ulcers, and intramural hematomas. The procedure aims to provide a minimally invasive alternative to open surgery, allowing for the effective reconstruction of the aortic arch and its branches. The study will assess the safety and efficacy of this technique, with key outcomes including the incidence of major adverse events (MAE) and the long-term success of the treatment.
Treatment: QYM Technique
Data and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- 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)
- Record updated
- 13 November 2026