Under construction – not a live service
Sign in
Taking people in ChinaNo phase

Clinical Trial of BAO-G Technique in Complex Aortic Aneurysm Endovascular Repair (BAO-G-02)

Key facts

Where
Beijing, Chongqing, Guangzhou, Haikou, Jining, Shanghai, and Zhengzhou, ChinaSee the 11 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07141251, who can take part

Where in China

  • Beijing Anzhen Hospital, Capital Medical UniversityBeijing, ChinaContact: Bao LiuTaking people
  • Fuwai Hospital ,CAMS&PUMCBeijing, ChinaContact: Bao LiuTaking people
  • Peking Union Medical College HospitalBeijing, ChinaContact: Bao LiuTaking people
  • The First Affiliated Hospital of Chongqing Medical UniversityChongqing, ChinaContact: Bao LiuTaking people
  • The First Affiliated Hospital, Sun Yat-sen UniversityGuangzhou, ChinaContact: Bao LiuTaking people
  • Hainan General HospitalHaikou, ChinaContact: Bao LiuTaking people
  • The Affiliated Hospital of Jining Medical UniversityJining, ChinaContact: Bao LiuTaking people
  • Changhai HospitalShanghai, ChinaContact: Bao LiuTaking people
  • Renji Hospital Shanghai Jiao Tong University School of MedicineShanghai, ChinaContact: Bao LiuTaking people
  • Zhongshan Hospital,Fudan UniversityShanghai, ChinaContact: Bao LiuTaking people
  • The First Affiliated Hospital of Zhengzhou UniversityZhengzhou, ChinaContact: Bao LiuTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Peking Union Medical College Hospital
Trial code
NCT07141251
Record updated
15 October 2026
Original description
Multi-Branch AOrtic Reconstruction With G-iliac System (BAO-G) Technique is a novel technique of endovascular repair of complex aortic aneurysm, which using off-the-shelf iliac branched devices to reconstruct the visceral branches. This study aims to verify the perioperative safety and 5-year efficacy of BAO-G technique in the endovascular treatment of complex aortic aneurysms through a prospective, multicenter, open-label, single-arm clinical trial, and to provide evidence for the selection of clinical procedures for complex aortic aneurysm patients in the future.Read full original descriptionShow less

Multicenter, Open-labeled, Single-arm Clinical Trial of Multi-Branch AOrtic Reconstruction of Complex Aortic Aneurysm With G-iliac System [BAO-G] Technique

Multi-Branch AOrtic Reconstruction With G-iliac System (BAO-G) Technique is a novel technique of endovascular repair of complex aortic aneurysm, which using off-the-shelf iliac branched devices to reconstruct the visceral branches. This study aims to verify the perioperative safety and 5-year efficacy of BAO-G technique in the endovascular treatment of complex aortic aneurysms through a prospective, multicenter, open-label, single-arm clinical trial, and to provide evidence for the selection of clinical procedures for complex aortic aneurysm patients in the future.

Inclusion: Diagnosed with Crawford type Ⅰ- Ⅴ thoracoabdominal aortic aneurysm or complex abdominal aortic aneurysm, with a healthy proximal landing zone (>20mm length, angulation <60°) in the descending aorta and maximum aneurysm diameter ≥4cm; Patients with pseudoaneurysms, post-dissection aneurysmal degeneration, or failure of previous EVAR were also eligible if the pathology involved the visceral aortic segment; Scheduled for endovascular aortic repair with commercially available iliac branch devices for visceral artery reconstruction; Signed informed consent and committed to protocol-defined follow-up.

Exclusion: Concurrent participation in other interventional clinical trials; Acquired language barrier, intellectual decline, cognitive impairment, or mental illness preventing informed consent; Uncontrolled autoimmune diseases (e.g., Takayasu arteritis, systemic lupus erythematosus, vasculitis); End-stage renal/hepatic/cardiac/pulmonary failure or malignancy diagnosed within 5 years, likely to cause mortality during follow-up; Active bleeding or coagulopathy within 6 months (high bleeding risk); Uncontrolled hypertension (resting SBP >180 mmHg or DBP >110 mmHg); Uncontrolled diabetes (fasting blood glucose >16.7 mmol/L); Severe hepatic/renal dysfunction (serum creatinine >3 mg/dL, ALT/AST >3×ULN); Pregnancy or perinatal status; Refusal to sign informed consent.

ClinicalTrials.gov NCT07141251