Transcranial Doppler Evaluation After Endovascular Thrombectomy for Acute Ischemic Stroke (PRECISE-TCD)
Part of paid clinical trials in Richmond, Virginia.
- Sponsor
- Virginia Commonwealth University
- Study ID
- NCT07013396
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Acute Ischemic Stroke
- Anterior Cerebral Artery Stroke
- Anterior Cerebral Artery Syndrome
- Cardioembolic Stroke
- Vasogenic Cerebral Edema
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Transcranial Doppler (TCD) examination — OTHERSerial non-invasive TCD monitoring will be performed as soon as possible after EVT, daily for 72 hours, and when possible, close to any neurological deterioration or head CT obtained within 72 hours after EVT. TCD parameters include PSV, EDV, MFV, and PI measured in bilateral MCA, ACA, PCA, carotid siphon, vertebrobasilar arteries, and ophthalmic artery territories. Collateralization patterns, including ACA flow reversal, ophthalmic artery flow reversal, and high-flow ACA or PCA patterns relative to MCA flow, will also be assessed.
Study Details
Endovascular thrombectomy (EVT) improves outcomes in acute ischemic stroke caused by large vessel occlusion. Despite successful recanalization, early neurological deterioration (END) remains frequent and is associated with poor outcomes. Transcranial Doppler (TCD) provides noninvasive, real-time assessment of cerebral blood flow velocities and may identify hemodynamic patterns associated with deterioration after EVT. PRECISE-TCD is a prospective, single-center observational study enrolling 180-300 patients undergoing EVT for anterior circulation large vessel occlusion at a tertiary academic medical center. Serial TCD examinations are performed immediately after EVT, daily for 72 hours, and as close as possible to early neurological deterioration events or clinically indicated head CT within 72 hours. The primary outcome is the association between TCD-derived hemodynamic parameters and END within 72 hours. Secondary outcomes include NIHSS at 24 hours and discharge, discharge disposition, and modified Rankin Scale at 90 days.
Key Dates
- First listed
- Jun 10, 2025
- Start date
- Aug 31, 2026
- Status verified
- Jul 2026
- Primary completion
- Aug 31, 2029
- Completion
- Aug 31, 2029
Study Design
- Enrollment
- 100 participants (estimated)
Arms
- Arm: Anterior circulation LVO stroke treated with EVTPatients with anterior circulation large vessel occlusion, including ACA, MCA, or ICA stroke, with tandem occlusions included, treated with endovascular thrombectomy at VCU Medical Center.
Primary Outcome Measure
Occurrence of early neurological deterioration (END) within 72 hours after EVT [ Time Frame: Within 72 hours after EVT ]
Central Contacts
- Tarun Srivastava804-828-9499
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Virginia Commonwealth University | Richmond | Virginia | 23235 | Aarti Sarwal Aarti Sarwal (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Richmond, VA
Related Studies
- Brain, Blood And Clot or Tissue Registry And CollaborationRecruiting · Justin Fraser · Lexington, Kentucky
- Quelling of Excitotoxicity in Acute Stroke With KetaminePHASE2/PHASE3 · Not Yet Recruiting · Lower Merion Neurology Research Foundation · Wynnewood, Pennsylvania
- A Study to Evaluate the Safety and Efficacy of LT3001 Drug Product in Subjects AIS Undergoing EVTPHASE2 · Recruiting · Lumosa Therapeutics Co., Ltd. · Chattanooga, Tennessee
- Proximal Internal Carotid Artery Acute Stroke Secondary to Tandem or Local Occlusion Thrombectomy TrialPHASE3 · Recruiting · Mercy Health Ohio · Mobile, Alabama