Stent Placement Clinical Trials

Clinical trials related to Stent Placement Procedure

Remote Ischemic Conditioning Plus Stenting for Symptomatic Carotid Artery Stenosis (RICSICAS): A Prospective, Randomized Controlled, Blind Endpoint, Single-Center Study

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Remote ischemic conditioning (RIC) has emerged as a promising non-invasive strategy to protect the brain, with evidence suggesting its benefit in patients with carotid artery stenting (CAS). However, the long-term benefit and safety of chronic RIC in this population remain unknown. This trial aims to evaluate whether chronic RIC reduces the incidence of major vascular events and improves clinical outcomes in high-risk patients with carotid artery stenosis who received CAS.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Healthy Volunteers: f
View:

• Age ≥ 40 years old;

• Patients with symptomatic moderate to severe stenosis of the internal carotid artery;

• History of ipsilateral cerebral ischemic symptoms within the past 180 days;

• Planned for carotid artery stent;

• Essen Score ≥ 3;

• Modified Rankin Scale score of 0 or 1;

• Signed informed consent.

Locations
Other Locations
China
Department of Neurology, General Hospital of Northern Theater Command
RECRUITING
Shenyang
Time Frame
Start Date: 2026-03-04
Estimated Completion Date: 2027-11-30
Participants
Target number of participants: 300
Treatments
Experimental: RIC group
The RIC protocol involves bilateral upper-arm cuff inflation to 200 mmHg (5-min inflation/5-min deflation, 5 cycles) performed 1-2 times daily, starting 3 days before CAS and continuing for 12 months post-procedure.
No_intervention: Control group
no RIC treatment
Related Therapeutic Areas
Sponsors
Leads: General Hospital of Shenyang Military Region

This content was sourced from clinicaltrials.gov