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Transcranial Doppler monitoring aims to reduce new DWI lesions by 50% in carotid stentingNew Trial Plans to Use TCD Monitoring for Carotid Stenosis

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Key Takeaway
Note that this is a trial protocol only; results regarding transcranial Doppler efficacy are not yet available.

This randomized controlled trial protocol describes a single-center study involving 232 patients scheduled for carotid artery stenting (CAS) due to severe internal carotid artery stenosis. The primary objective is to evaluate the efficacy of transcranial Doppler (TCD) monitoring as an adjuvant therapy during the procedure.

The intervention group receives TCD monitoring (1.6 MHz, 0.274 MPa) from the femoral artery puncture until 30-60 minutes after procedure completion plus standard care. The comparator group receives standard care alone. The primary outcome is the number of new diffusion-weighted imaging (DWI) lesions at 24 hours post-randomization. Secondary outcomes include intracranial hemorrhage within 24 hours.

The study anticipates a 50% reduction in new DWI lesions, moving from an expected rate of 2.0 to 1.0. No actual results are reported as the trial is currently in the protocol stage. Safety endpoints focus on intracranial hemorrhage within 24 hours post-randomization.

A major limitation is that this is a protocol and design study; therefore, no clinical data or outcomes have been collected yet. The trial aims to determine if TCD monitoring can reduce cerebral embolic events during carotid intervention. Clinical application of these findings cannot be determined until the trial is completed.

Researchers are preparing a study to evaluate a specific monitoring technique for patients undergoing carotid artery stenting. This procedure is used to treat severe narrowing of the internal carotid artery. The study will involve 232 patients who are scheduled for this surgery.

The trial plans to use transcranial Doppler (TCD) monitoring as an extra layer of care. This method involves tracking blood flow from the time a femoral artery is punctured until about 30 to 60 minutes after the procedure ends. The goal is to see if this additional monitoring can reduce the number of new brain lesions that occur during the operation.

Because this is currently a trial protocol, no final results are available yet. The study is designed to check both the effectiveness of TCD and its safety regarding intracranial hemorrhage. Since the study has not been completed, these findings cannot be used to change current medical practices at this time.

What this means for you:
This is a planned study; results on whether TCD monitoring reduces brain lesions are not yet available.

Common questions

What is being tested in this study?

The study is testing whether transcranial Doppler (TCD) monitoring can serve as an extra tool during carotid artery stenting. The goal is to see if this method helps reduce the number of new brain lesions that occur in patients with severe internal carotid artery stenosis.

Are there results available from this study yet?

No, results are not available yet because this is a trial protocol. This means it is a plan for a future study rather than a report of completed research. The researchers have not yet conducted the procedures to collect data.

Who is eligible for this specific trial?

The study is designed for patients who are already scheduled for carotid artery stenting due to severe internal carotid artery stenosis. The plan involves a group of 232 patients at a single center.

Study Details

Study typeRct
EvidenceLevel 2
PublishedAug 2026
View Original Abstract ↓
BackgroundCarotid artery stenting (CAS) is an effective revascularization procedure for internal carotid artery stenosis, but it is associated with a high incidence of perioperative cerebral embolism, with asymptomatic and symptomatic embolic events occurring in up to 40% of patients. Transcranial Doppler (TCD) has been shown to enhance fibrinolysis through sonothrombolysis and may reduce embolic burden during carotid interventions.AimsTo evaluate whether intraoperative and post-procedural TCD monitoring can reduce the number of new diffusion-weighted imaging (DWI) lesions after CAS in patients with severe internal carotid artery stenosis.Sample size estimatesA total of 232 patients are required to detect a 50% reduction in the median number of new DWI lesions (from 2.0 to 1.0) with 80% power and a two-sided α of 0.05, accounting for a 5% dropout rate.DesignTCD-ICAS is a prospective, randomized, single-center, blinded endpoint trial. Patients scheduled for CAS are randomized 1:1 to receive either TCD treatment (1.6 MHz, 0.274 MPa) from femoral artery puncture until 30–60 min after procedure completion plus standard care, or standard care alone.OutcomesThe primary efficacy endpoint is the number of new DWI lesions at 24 h post-randomization. The primary safety endpoint is intracranial hemorrhage within 24 h.ConclusionThe TCD-ICAS trial will assess the efficacy and safety of TCD as an adjuvant therapy to reduce cerebral embolic events in patients undergoing CAS.Clinical trial registrationIdentifier (NCT07462546).
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