Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06823128

Safety and Efficacy of Remote Ischemic Conditioning in Patients with Severe Stenosis or Occlusion of Anterior Intracranial Circulation Vessels

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
1,000 (estimated)
Sponsor
The First Affiliated Hospital of University of Science and Technology of China · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary purpose of this study is to examine whether remote ischemic treatment can better the 90 - day neurological outcomes in acute ischemic stroke patients having severe stenosis or occlusion of anterior intracranial circulation vessels.

Conditions

Interventions

TypeNameDescription
DEVICERICRemote Ischemic Conditioning is given twice a day with 200mmHg pressure,last for 7 to 10 days.
DEVICEShamRIC is given twice a day with 60mmHg pressure, last for 7 to 10 days.
OTHERGuideline-based therapyGuideline-based therapy

Timeline

Start date
2025-02-01
Primary completion
2025-02-01
Completion
2027-02-01
First posted
2025-02-12
Last updated
2025-02-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06823128. Inclusion in this directory is not an endorsement.