Open and Endovascular Surgical Treatment for Artery Injuries
Primary Purpose
Artery Injury
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Endovascular treatment
Open surgery
Sponsored by
About this trial
This is an interventional treatment trial for Artery Injury focused on measuring Artery Injury, Surgery, Endovascular Repair, Peripheral Arteries
Eligibility Criteria
Inclusion Criteria:
Injuries in the peripheral arteries; Loss of blood supply to the remote area; High-risk emergency artery reconstruction; Participate in the study voluntarily, accept follow up study. -
Exclusion Criteria:
Bleeding can be easily control; There is contraindications for surgical operation. -
Sites / Locations
- 960 Hospital of PLARecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Endovascular treatment
Open surgery
Arm Description
Outcomes
Primary Outcome Measures
5-year treatment success rate
Treatment success is defined as restored blood flow without clinical complications.
Secondary Outcome Measures
Technically success rate of surgery
Surgery-related complications or death
Currence of stenosis of target lesion
Device-related serious adverse events
Target lesion was treated by interventional or surgical therapy once again
Full Information
NCT ID
NCT03872323
First Posted
March 11, 2019
Last Updated
March 11, 2019
Sponsor
Jinan Military General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03872323
Brief Title
Open and Endovascular Surgical Treatment for Artery Injuries
Official Title
Comparison Between Open and Endovascular Surgical Techniques to Manage Vascular Injuries
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2019 (Anticipated)
Primary Completion Date
April 30, 2024 (Anticipated)
Study Completion Date
January 1, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jinan Military General Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Traumatic injuries of peripheral arteries are often associated with multiple injuries, massive hemorrhage, state of shock, and loss of blood supply, as well as with high mortality. Traditionally, an open surgical approach is suggested for the management of artery injury. With the advancement of endovascular techniques, the traditional open vascular exposure and vessel repair are no longer the only option available. The purpose of this study is to compare the effectiveness, long-term safety and explore the safety and efficacy factors between open and endovascular surgical techniques.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Artery Injury
Keywords
Artery Injury, Surgery, Endovascular Repair, Peripheral Arteries
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Non-Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Endovascular treatment
Arm Type
Active Comparator
Arm Title
Open surgery
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Endovascular treatment
Intervention Description
The arteries injuries are repaired by endovascular treatment.
Intervention Type
Procedure
Intervention Name(s)
Open surgery
Intervention Description
The arteries injuries are repaired by open surgical operation.
Primary Outcome Measure Information:
Title
5-year treatment success rate
Description
Treatment success is defined as restored blood flow without clinical complications.
Time Frame
60 months
Secondary Outcome Measure Information:
Title
Technically success rate of surgery
Time Frame
immediately after surgery
Title
Surgery-related complications or death
Time Frame
60 months
Title
Currence of stenosis of target lesion
Time Frame
60 months
Title
Device-related serious adverse events
Time Frame
60 months
Title
Target lesion was treated by interventional or surgical therapy once again
Time Frame
60 months
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Injuries in the peripheral arteries; Loss of blood supply to the remote area; High-risk emergency artery reconstruction; Participate in the study voluntarily, accept follow up study. -
Exclusion Criteria:
Bleeding can be easily control; There is contraindications for surgical operation. -
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Min Li, M.D.
Phone
13953176057
Email
liminyingxiang@163.com
Facility Information:
Facility Name
960 Hospital of PLA
City
Jinan
State/Province
Shandong
ZIP/Postal Code
250031
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Min Li, M.D.
12. IPD Sharing Statement
Learn more about this trial
Open and Endovascular Surgical Treatment for Artery Injuries
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