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Safety and Efficacy of the Minimally Invasive Bentall Procedure Via a Small Right Intercostal Incision in Patients With Aortic Root Lesions

Safety and Efficacy of the Minimally Invasive Bentall Procedure Via a Small Right Intercostal Incision in Patients With Aortic Root Lesions: an Investigator-initiated, Single-center, Retrospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06177548
Acronym
Mini-Bentall
Enrollment
350
Registered
2023-12-20
Start date
2023-12-11
Completion date
2024-12-28
Last updated
2024-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Dissection, Aortic Root Aneurysm, Minimally Invasive Surgical Procedures

Brief summary

This study intends to include patients who had aortic root lesions and were treated with Bentall surgery from January 2019 to July 2023 in the First Affiliated Hospital of Xi'an Jiaotong University. The patients will be divided into the minimally invasive group and control group according to the surgical methods: the former underwent minimally invasive Bentall surgery through a small right intercostal incision; the latter underwent traditional Bentall surgery through a median sternal incision. By comparing the clinical data of patients in two groups, we will investigate the effect and safety of minimally invasive Bentall surgery.

Interventions

PROCEDUREMinimally invasive Bentall procedure

The minimally invasive Bentall procedure is performed through a small incision in the right intercostal space.

Sponsors

First Affiliated Hospital Xi'an Jiaotong University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- Patients who were diagnosed with aortic root lesions and treated with the Bentall procedure at the First Affiliated Hospital of Xi'an Jiaotong University from January 2019 to July 2023 will be included in this study.

Exclusion criteria

* Previous sternotomy or aortic root surgery; * Combined coronary artery disease requiring simultaneous coronary revascularization; * Combined aortic arch lesions requiring simultaneous aortic arch surgery; * Preoperative comorbidities with severe single or multiple organ failure; * Incomplete clinical information;

Design outcomes

Primary

MeasureTime frameDescription
30-day mortality rate1-month after the operation.It focuses on the mortality rate of all patients after the operation after 30 days. The data will be obtained from medical records.

Secondary

MeasureTime frameDescription
Mortality rate during hospitalizationAbout 10 days after the operation.It focuses on the mortality rate of all patients after the operation during hospitalization. The data will be obtained from medical records.
Blood transfusion volume during hospitalizationAbout 10 days after the operation.It focuses on the blood transfusion volumes of all patients after the operation during hospitalization. The data will be obtained from medical records.
Postoperative ICU length of stayAbout 3 days after the operation.It focuses on the ICU length of stay of all patients after the operation. The data will be obtained from medical records.
Postoperative ventilation timeAbout 1 day after the operation.It focuses on the postoperative ventilation time of all patients after the operation. The data will be obtained from medical records.

Countries

China

Contacts

Primary ContactYan Yang
yangyan3@xjtu.edu.cn+86.29.85323869
Backup ContactLi Guoliang
liguoliang_med@163.com+86.29.85323869

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026