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Effect of Remote Ischemic Preconditioning on Cerebral Circulation Time in Patients With Severe Carotid Artery Stenosis (RIP-CCT) - Trial NCT05451030

Access comprehensive clinical trial information for NCT05451030 through Pure Global AI's free database. This phase not specified trial is sponsored by General Hospital of Shenyang Military Region and is currently Recruiting. The study focuses on Carotid Artery Stenosis. Target enrollment is 122 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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ClinicalTrials.gov โ€ข NCT05451030
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Effect of Remote Ischemic Preconditioning on Cerebral Circulation Time in Patients With Severe Carotid Artery Stenosis (RIP-CCT)
The Effect of Remote Ischemic Preconditioning on Cerebral Circulation Time in Patients With Severe Carotid Artery Stenosis (RIP-CCT): A Prospective, Randomized Controlled, Blind Outcome Evaluation, Multi-center Study

Study Focus

Carotid Artery Stenosis

remote ischemic preconditioning

Interventional

device

Sponsor & Location

General Hospital of Shenyang Military Region

Shenyang, China

Timeline & Enrollment

N/A

Jun 28, 2022

Jun 28, 2023

122 participants

Primary Outcome

Changes in cerebral circulation time

Summary

Cerebral circulation time in patients with severe carotid artery stenosis was found to be
 associated with hyperperfusion syndrome. Remote ischemic preconditioning can change the
 ability of cerebral autoregulation. The prospective, randomized controlled, blind outcome
 evaluation, multi-center study aimed to investigate the effect of remote ischemic
 preconditioning on cerebral circulation time in patients with severe carotid artery stenosis.

ICD-10 Classifications

Occlusion and stenosis of carotid artery
Carotid artery syndrome (hemispheric)
Injury of carotid artery
Aneurysm and dissection of carotid artery
Occlusion and stenosis of vertebral artery

Data Source

ClinicalTrials.gov

NCT05451030

Device Trial