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Tenecteplase for Thrombolysis Bridging Thrombectomy Combined with Remote Ischemia Conditioning in Acute Ischemic Stroke

Tenecteplase for Thrombolysis Bridging Thrombectomy Combined with Remote Ischemia Conditioning in Acute Ischemic Stroke

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073033
Enrollment
Unknown
Registered
2023-06-30
Start date
2023-06-30
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Cerebrovascular diseases

Interventions

RIC group:The patient received bilateral upper limb RIC (cuff pressure 180mmHg) twice a day for at least 7 consecutive days within 48 hours after operation. An entire intervention episode is composed
Conventional treatment group:Accept standardized diagnosis and treatment plans recommended by the guidelines

Sponsors

the First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to No maximum

Inclusion criteria

Inclusion criteria: ? Adults (age = 18 years old); ? Patients received teneplase thrombolytic (0.25mg/kg, maximum 25mg) followed by thrombectomy within 6 hours after onset or when the onset time was unknown but DWI and FLAIR imaging mismatching; ? Patients diagnosed with anterior circulation LVO-AIS by DSA (anterior circulation LVO was defined as occlusion of the internal carotid artery or the M1 and M2 segments of the middle cerebral artery); ? Premorbid mRS score =2; ? Patients or their legal representatives signed the informed consent.

Exclusion criteria

Exclusion criteria: ? Intracranial hemorrhage showed by cranial imaging examination within 24-36 hours after operation; ? The modified Thrombolysis in Cerebral Infarction grade after operation lower than 2b grade; ? Postoperative hemodynamic instability (blood pressure below 90/60mmHg or above 200/110mmHg after treatment); ? Pregnant or breastfeeding women; ? Any contraindications for RIC,such as severe soft tissue injury, fracture, thrombotic diseases, confirmed peripheral vascular lesions, active visceral bleeding, acute phase of fundus hemorrhage, cerebral aneurysms and cerebral arteriovenous malformations, or other situations deemed unsuitable for RIC treatment by researchers; ? Patients with a life expectancy of fewer than 90 days, or unwilling to be followed up.

Design outcomes

Primary

MeasureTime frame
The proportion of patients with favorable functional outcomes (mRS=2) at 90 days;

Secondary

MeasureTime frame
The neurological function (NIHSS and ADL scores) and cognitive function (MMSE and MoCA scores) of patients at 7 days;The neurological function (NIHSS and ADL scores) and cognitive function (MMSE and MoCA scores) of patients at 90 days;The neurological function (NIHSS and ADL scores) and cognitive function (MMSE and MoCA scores) of patients at 6 monthss;The proportion of patients with favorable functional outcomes (mRS=2) at 6 months;The proportion of patients with stroke recurrence within 6 months;The collateral circulation compensation of cerebral blood flow of patients at 6 months;Dynamic changes of HIF-1a, bFGF, vEGF, S100-ß and NSE in blood;

Countries

China

Contacts

Public ContactYawen Cheng

the First Affiliated Hospital of Xi'an Jiaotong University

alicia_cheng@126.com+86 135 7227 5252

Outcome results

None listed

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