Thrombolysis and RIPC in Acute Ischemic Stroke (tripcais)

Xi'an Jiaotong University

Status: Completed

Conditions: Acute Ischemic Stroke, Cerebral Embolism and Thrombosis

Treatments: Device: RIPC device (IPC-906X)

Study type: Interventional

Funder types: Other

Identifiers

NCT03218293

XJTU1AF-CRF-2016-013

Details and patient eligibility

About

Remote ischemic postconditioning (RIPC) is suggested to protect the cerebral cell against ischemia in various settings. However, the effect of RIPC in patients with acute ischemic stroke who undergo thrombolysis has yet to be examined. In this single-center, randomized controlled trial, we examined the effect of RIPC on the resolution of nerve function deficient in response to thrombolysis. Patients in the RIPC group had five cycles of 5-min cuff inflation followed by 3-min deflation to the bilateral upper arm after thrombolysis. The primary endpoint was the recovery of nerve function deficient assessed by National Institutes of Health Stroke Scale(NIHSS), Activities of Daily Living(ADL), Modified Rankin Scale(mRS), CT cerebral perfusion imaging (CTP) and CT angiography(CTA). Secondary endpoints included the following: angiogenesis assessed by the level of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF).

Enrollment: 68 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• In accordance with the Guideline of Thrombolysis in Acute Ischemic Stroke and accomplish intravenous thrombolytic therapy using alteplase;
• The consciousness of patients are conscious,somnolence,confusion and stupor，can comply better with the RIPC treatment;
• Acute ischemic stroke confirmed by cranial CT/MRI;
• Provision of written informed consent.

Exclusion criteria

• History of cerebral embolism,cerebral hemorrhage, brain tumor, brain trauma or other brain lesion;
• Severe cardiac, liver, or kidney disease, malignancy, systemic organ dysfunction;
• Blood pressure <90/60 mmHg or >200/110 mmHg after treatment;
• Dementia or mental illness;
• History of major surgery or trauma 4 weeks prior to admission;
• Failure to provide informed consent.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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68 participants in 2 patient groups

RIPC

Experimental group

Description:

Remote ischemic postconditioning（RIPC）：Patients in the RIPC group not only receive foundational treatment but also have five cycles of 5-min cuff inflation followed by 3-min deflation to the bilateral upper arm using a RIPC device (IPC-906X; Beijing Renqiao Institute of Neuroscience, Beijing, China) after thrombolysis while in-hospital.

Treatment:

Device: RIPC device (IPC-906X)

Blank control group(BC)

No Intervention group

Description:

Blank control group:Patients in the BC group only receive foundational treatment, including free radical elimination in the acute stage, blood pressure and blood glucose stabilization, and antiplatelet (aspirin, 100-300 mg/d) and lipid-lowering (atorvastatin, 20 mg/d) drugs,throughout the 14 days in-hospital period without remote ischemic postconditioning after thrombolysis.