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Prehospital Remote Ischemic Conditioning in Patients with Acute Stroke

Prehospital Remote Ischemic Conditioning in Patients with Acute Stroke

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061406
Enrollment
Unknown
Registered
2022-06-23
Start date
2022-07-10
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

Intervention group:The patient's healthy upper limb was adapted to remote ischemia of 200mmhg, inflated for 5 minutes, deflated for 5 minutes as a cycle, and a total of 4 cycles were completed
Control group:The patient's healthy upper limb was isolated from ischemia and adapted to 0mmhg. The patient was bound for 40 minutes and simulated to complete 4 cycles

Sponsors

Beijing Emergency Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Adults aged over 18 years; 2. Suspected acute stroke was judged by the pre-hospital doctor; 3. From the onset of stroke symptoms (the patient's last normal time) to the randomization time of ambulance physicians within 12 hours; 4. Prehospital great vessel occlusion score G-FAST>=3 points; 5. Informed consent signed by the patient himself or his family.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications for intravascular interventional therapy (such as contrast media, peripheral artery occlusion, etc.) and unable to perform mechanical thrombectomy; 2. mRS (modified Rankin scale score) >2 before the onset of the stroke; 3. Patients with the previous responsible side cerebral artery occlusion; 4. History suggests apoplexy due to arterial dissection; 5. Dementia patients; 6. Patients who are breastfeeding or pregnant; 7. Severe renal insufficiency requiring dialysis or creatinine clearance < 29 mL/min; 8. Patients with severe systemic diseases and expected survival time of no more than 3 months; 9. Contraindications of distal ischemia adaptation: known upper limb peripheral vascular diseases such as severe soft tissue injury, fracture and sensory disturbance; 10. The researcher believed that the patient had other conditions that could not be included in the group.

Design outcomes

Primary

MeasureTime frame
Infarct size 7 days after onset of acute ischemic stroke;

Secondary

MeasureTime frame
Proportion of patients with good neurological function (modified Rankin scale, mRS, 0-2 points) 90 days after onset;Distribution of mRS at 90 days after onset;G-FAST score during pre hospital reception and after arrival and before handover;National Institutes of Health Stroke Scale (NIHSS) score on the 7th day of admission;90 day all-cause mortality;

Countries

China

Contacts

Public ContactLi Dou
lidou86@126.com+86 13501084639

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026