Skip to main content
Clinical Trials/NCT07288164
NCT07288164CompletedNot Applicable

Comparison of Operative and Early Postoperative Outcomes Between Eversion and Conventional Techniques in Carotid Endarterectomy

Kastamonu University1 site in 1 country129 target enrollmentStarted: May 15, 2025Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
129
Locations
1
Primary Endpoint
Number of participants with symptoms of occlusion

Study Overview

Brief Summary

Atherosclerotic carotid artery disease is responsible for approximately 20% of strokes worldwide, and its treatment options include medical therapy, surgery, and stenting.Surgical management is prioritized over medical and stent based approaches and can be performed using either the conventional methed closed primarily or with a patch or the eversion technique.The aim of this study was to compare the intraoperative and early postoperative outcomes of the eversion technique and the conventional method with primary closure.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients undergoing isolated carotid endarterectomy, either emergently or electively

Exclusion Criteria

  • Patients younger than 18 years of age
  • Patients scheduled for concomitant cardiac surgery
  • Reoperations

Arms & Interventions

Conventional endarterectomy

Who were performed conventional,primarily endarterectomy patients are included this group

Intervention: Carotid endarterectomy, conventional (Procedure)

Eversion

Who were performed eversion endarterectomy patients are included this group

Intervention: Carotid endarterectomy, eversion (Procedure)

Outcomes

Primary Outcomes

Number of participants with symptoms of occlusion

Time Frame: Postoperative 30 days

Early carotid restenosis or occlusion within 30 days after surgery

Number of participants with stroke and death

Time Frame: 30 days

All strokes and/or deaths occurring within 30 days after surgery

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

İsmail DAL

Assistant Professor Literally: Doctor Teaching Member

Kastamonu University

Study Sites (1)

Loading locations...

Similar Trials