Thrombectomy Clinical Trials

Clinical trials related to Thrombectomy Procedure

Tenecteplase or Reteplase as Bridging Thrombolysis Before Thrombectomy in Acute Ischemic Cerebrovascular Events (TRACE-BRIDGE): A Multicenter, Randomized, Open-Label, Three-Arm, Blinded-Endpoint Phase III Trial

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Acute ischemic stroke caused by large vessel occlusion (LVO) is a major cause of disability, and mechanical thrombectomy (MT) has become the standard treatment for eligible patients. However, the optimal role of intravenous thrombolysis before MT remains uncertain. The TRACE-BRIDGE trial is a phase 3, investigator-initiated, multicenter, randomized, open-label trial with blinded outcome assessment (PROBE design) evaluating different bridging thrombolysis strategies before MT. The trial will enroll adults with acute ischemic stroke presenting within 4.5 hours of symptom onset and with imaging-confirmed anterior circulation LVO who are eligible for intravenous thrombolysis and MT. Participants will be randomly assigned in a 1:1:1 ratio to receive tenecteplase plus MT, reteplase plus MT, or direct MT alone. The TRACE-BRIDGE trial aims to evaluate the efficacy and safety of bridging thrombolysis with tenecteplase or reteplase before mechanical thrombectomy compared with direct mechanical thrombectomy. The primary outcome is functional independence, defined as a modified Rankin Scale score of 0-2 at 90 days after randomization. If superiority of bridging thrombolysis is demonstrated, the trial will further evaluate whether reteplase is non-inferior to tenecteplase as a bridging thrombolytic strategy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with acute ischemic stroke presenting within 4.5 hours of symptom onset who are eligible for intravenous thrombolytic therapy. A baseline non-contrast CT or MRI is required for screening.

• Large vessel occlusion on computed tomographic angiography (CTA) or magnetic resonance angiography (MRA) of the intracranial carotid artery (ICA) or middle cerebral artery (MCA) M1

• Age ⩾ 18 years at the time of signing the informed consent form

• ASPECTS 6-10

• Informed consent from the patients or their legal representative.

Locations
Other Locations
China
Beijing Tiantan Hospital, Capital Medical Universiity
RECRUITING
Beijing
Rizhao Hospital of Traditional Chinese Medicine
NOT_YET_RECRUITING
Rizhao
Zhongnan Hospital of Wuhan University
NOT_YET_RECRUITING
Wuhan
Xiangtan Central Hospital
NOT_YET_RECRUITING
Xiangtan
Ya'an People's Hospital
NOT_YET_RECRUITING
Ya'an
Contact Information
Primary
Yongjun Wang, MD
yongjunwang@ncrcnd.org.cn
+86 13911172565
Backup
Bowei Zhang, MD
boweizhang@ncrcnd.org.cn
+86 13001139469
Time Frame
Start Date: 2026-10-16
Estimated Completion Date: 2029-08-01
Participants
Target number of participants: 1440
Treatments
Experimental: rhTNK-tPA+MT
Recombinant human TNK tissue-type plasminogen activator for injection (rhTNK-tPA) administered as a single intravenous bolus at a dose of 0.25 mg/kg (maximum dose 25 mg) within 4.5 hours of symptom onset and prior to mechanical thrombectomy, followed by standard endovascular treatment.
Experimental: rPA+MT
Recombinant human plasminogen activator derivative (rPA) administered as two intravenous bolus doses of 18 mg each, given over approximately 2 minutes per bolus and separated by a 30-minute interval. The first dose should be administered within 4.5 hours of symptom onset before mechanical thrombectomy. To avoid delays in reperfusion therapy, groin puncture and endovascular treatment may be initiated after administration of the first bolus without waiting for the second dose. The second bolus should be administered according to the prespecified dosing regimen unless contraindicated.
Active_comparator: MT alone
Mechanical thrombectomy performed according to standard practice without administration of intravenous thrombolytic agents.
Related Therapeutic Areas
Sponsors
Leads: Yongjun Wang

This content was sourced from clinicaltrials.gov

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