Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT03669653

Safety and Efficacy of Remote Ischemic Conditioning in Patients With Acute Ischemic Stroke

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
912 (estimated)
Sponsor
Yi Yang · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

he purpose of this study is to determine the efficacy and safety of remote ischemic conditioning for acute ischemic stroke.

Detailed description

In this study, 912 cases of ischemic stroke in 48 hours were included in 5 centers in China according to the principle of random, double-blind and parallel control .The experimental group receive basic treatment and remote ischemic conditioning for 200mmHg, 2 times per day for 7 consecutive days .The control group receive basic treatment and remote ischemic conditioning control for 60mmHg, 2 times per day, 7 days in a row . Two groups will be followed up for 90 days to evaluate the efficacy and safety of remote ischemic conditioning therapy.

Conditions

Interventions

TypeNameDescription
PROCEDURERemote ischemic conditioningRemote ischemic conditioning (RIC) is induced by 4 cycles of 5 min of healthy upper limb ischemia followed by 5 min reperfusion. Limb ischemia was induced by inflations of a blood pressure cuff to 200 mm Hg. RIC will be conducted twice daily for 7 days.
PROCEDURESham remote ischemic conditioningRemote ischemic conditioning (RIC) is induced by 4 cycles of 5 min of healthy upper limb ischemia followed by 5 min reperfusion. Limb ischemia was induced by inflations of a blood pressure cuff to 60 mm Hg. RIC will be conducted twice daily for 7 days.

Timeline

Start date
2025-06-17
Primary completion
2026-09-20
Completion
2026-09-20
First posted
2018-09-13
Last updated
2024-10-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03669653. Inclusion in this directory is not an endorsement.