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Clinical Trial Summary

This study aims to evaluate the prognosis of patients with spontaneous solitary dissection of superior mesenteric artery (SIDSMA) who have been treated with stents.


Clinical Trial Description

This study is an observational study. The subject's treatment plan needs to be expected to meet the following conditions: the corresponding surgery has been completed: the femoral artery or brachial artery approach is implanted into the true lumen of the SMA bare stent (the part with a diameter ≤ 7mm is above the 100-strong stent, and the part with a diameter> 7mm It is not limited to using stents (brands) to restore the real lumen blood flow of the superior mesenteric artery. If the false cavity is large, it can be combined with a spring coil to assist embolization. Anticoagulation therapy for at least 1 day after surgery, anticoagulation drugs are not limited to use, and discharge After taking the double antibody for 3 months, the monoclonal antibody should be maintained for at least 1 year. ;


Study Design


Related Conditions & MeSH terms

  • Dissection of the Superior Mesenteric Artery

NCT number NCT05171842
Study type Observational
Source First Affiliated Hospital of Zhejiang University
Contact Hongkun zhang
Phone 0571-87236745
Email 1198050@zju.edu.cn
Status Recruiting
Phase
Start date September 9, 2021
Completion date December 1, 2025

See also
  Status Clinical Trial Phase
Active, not recruiting NCT03916965 - Stent Implantation for Patients With SIDSMA