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
| Type | Name | Description |
|---|---|---|
| DEVICE | RIC | Remote Ischemic Conditioning is given twice a day with 200mmHg pressure,last for 7 to 10 days. |
| DEVICE | Sham | RIC is given twice a day with 60mmHg pressure, last for 7 to 10 days. |
| OTHER | Guideline-based therapy | Guideline-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.