Expertise in
53
conditions

Dr. Ricardo A. Hanel

Neurosurgery
Lyerly Baptist Inc
800 Prudential Dr, 
Jacksonville, FL 
Accepting New Patients
Offers Telehealth
Expertise in
53
conditions
Lyerly Baptist Inc
800 Prudential Dr, 
Jacksonville, FL 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

Ricardo Hanel is a Neurosurgery provider in Jacksonville, Florida. Dr. Hanel is highly rated in 53 conditions, according to our data. His top areas of expertise are Brain Aneurysm, Stroke, Subdural Hematoma, Thrombectomy, and Stent Placement. Dr. Hanel is currently accepting new patients.

His clinical research consists of co-authoring 276 peer reviewed articles and participating in 17 clinical trials. MediFind looks at clinical research from the past 15 years.

Specialties
Neurosurgery
Licenses
Neurological Surgery in FL
Hospital Affiliations
Baptist Medical Center - Nassau
Baptist Health Medical Center - Jacksonville
Southeast Georgia Health System- Brunswick Campus
Baptist Medical Center Beaches
Languages Spoken
English
Gender
Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Florida Blue
  • EPO
  • PPO
Health Options
  • HMO
  • POS
  • PPO
Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO

Locations

LYERLY BAPTIST INC
800 Prudential Dr, Jacksonville, FL 32207
Other Locations
LYERLY BAPTIST INC
1370 13th Ave S, Suite 215, Jacksonville Beach, FL 32250

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

17 Clinical Trials

Embotrap eXtraction & Clot EvaLuation & Lesion Evaluation for NeuroThrombectomy
Embotrap eXtraction & Clot EvaLuation & Lesion Evaluation for NeuroThrombectomy
Enrollment Status: Completed
Publish Date: June 03, 2025
Intervention Type: Device
Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trial
Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trial
Enrollment Status: Active_not_recruiting
Publish Date: May 14, 2025
Intervention Type: Device, Other, Procedure
Study Phase: Not Applicable
A Prospective, Randomized, Controlled, Interventional Clinical Trial to Evaluate the Safety and Effectiveness of the Route 92 Medical MonoPoint® Reperfusion System for Aspiration Embolectomy in Acute Ischemic Stroke Patients (SUMMIT MAX)
A Prospective, Randomized, Controlled, Interventional Clinical Trial to Evaluate the Safety and Effectiveness of the Route 92 Medical MonoPoint® Reperfusion System for Aspiration Embolectomy in Acute Ischemic Stroke Patients (SUMMIT MAX)
Enrollment Status: Completed
Publish Date: April 09, 2025
Intervention Type: Device
Study Phase: Not Applicable
US IDE Study of the Contour NEurovasCular System™ for IntraCranial Aneurysm Repair
US IDE Study of the Contour NEurovasCular System™ for IntraCranial Aneurysm Repair
Enrollment Status: Active_not_recruiting
Publish Date: December 20, 2024
Intervention Type: Device
Study Phase: Phase 4
SELECT2: A Randomized Controlled Trial to Optimize Patient's Selection for Endovascular Treatment in Acute Ischemic Stroke
SELECT2: A Randomized Controlled Trial to Optimize Patient's Selection for Endovascular Treatment in Acute Ischemic Stroke
Enrollment Status: Completed
Publish Date: November 21, 2024
Intervention Type: Other, Device
Study Phase: Not Applicable
Success in Comaneci-assist Coils Embolization Surveillance Study
Success in Comaneci-assist Coils Embolization Surveillance Study
Enrollment Status: Completed
Publish Date: November 14, 2024
Intervention Type: Device
A Phase 3, Multicenter, Open-Label, Single-Arm Study of Bentracimab (PB2452) in Ticagrelor-Treated Patients With Uncontrolled Major or Life-Threatening Bleeding or Requiring Urgent Surgery or Invasive Procedure (REVERSE-IT Trial)
A Phase 3, Multicenter, Open-Label, Single-Arm Study of Bentracimab (PB2452) in Ticagrelor-Treated Patients With Uncontrolled Major or Life-Threatening Bleeding or Requiring Urgent Surgery or Invasive Procedure (REVERSE-IT Trial)
Enrollment Status: Completed
Publish Date: October 21, 2024
Intervention Type: Drug
Study Phase: Phase 3
Treatment With Intent to Generate Endovascular Reperfusion
Treatment With Intent to Generate Endovascular Reperfusion
Enrollment Status: Completed
Publish Date: May 08, 2024
Intervention Type: Device
Study Phase: Not Applicable
ENRICH: A Multi-center, Randomized, Clinical Trial Comparing Standard Medical Management to Early Surgical Hematoma Evacuation Using Minimally Invasive Parafascicular Surgery (MIPS) in the Treatment of Intracerebral Hemorrhage (ICH).
ENRICH: A Multi-center, Randomized, Clinical Trial Comparing Standard Medical Management to Early Surgical Hematoma Evacuation Using Minimally Invasive Parafascicular Surgery (MIPS) in the Treatment of Intracerebral Hemorrhage (ICH).
Enrollment Status: Completed
Publish Date: May 10, 2023
Intervention Type: Procedure
Study Phase: Not Applicable
Safety and Effectiveness of the Treatment of Wide Neck, Intracranial, Saccular Aneurysms With the Next Generation Neuroform Stent System
Safety and Effectiveness of the Treatment of Wide Neck, Intracranial, Saccular Aneurysms With the Next Generation Neuroform Stent System
Enrollment Status: Completed
Publish Date: March 24, 2023
Intervention Type: Device
Study Phase: Not Applicable
Pivotal Study of the MicroVention, Inc. Carotid Artery Stent System Used in Conjunction With the Nanoparasol® Embolic Protection System for the Treatment of Carotid Artery Stenosis in Patients at Elevated Risk for Adverse Events From Carotid Endarterectomy.(CONFIDENCE Trial)
Pivotal Study of the MicroVention, Inc. Carotid Artery Stent System Used in Conjunction With the Nanoparasol® Embolic Protection System for the Treatment of Carotid Artery Stenosis in Patients at Elevated Risk for Adverse Events From Carotid Endarterectomy.(CONFIDENCE Trial)
Enrollment Status: Unknown
Publish Date: February 28, 2023
Intervention Type: Device
Study Phase: Not Applicable
The Vesalio Neva VS for the Treatment of Symptomatic Cerebral Vasospasm Following Aneurysmal Subarachnoid Hemorrhage (aSAH) (The VITAL Study)
The Vesalio Neva VS for the Treatment of Symptomatic Cerebral Vasospasm Following Aneurysmal Subarachnoid Hemorrhage (aSAH) (The VITAL Study)
Enrollment Status: Completed
Publish Date: January 03, 2023
Intervention Type: Device
Study Phase: Not Applicable
Pivotal Study of the MicroVention Flow Re-Direction Endoluminal Device (FRED) Stent System in the Treatment of Intracranial Aneurysms
Pivotal Study of the MicroVention Flow Re-Direction Endoluminal Device (FRED) Stent System in the Treatment of Intracranial Aneurysms
Enrollment Status: Completed
Publish Date: March 08, 2021
Intervention Type: Device
Study Phase: Not Applicable
A Prospective, Multi-center, Single Arm Study to Evaluate the Safety and Effectiveness of the CODMAN ENTERPRISE® Vascular Reconstruction Device and Delivery System When Used in Conjunction With Endovascular Coil Embolization in the Treatment of Wide-necked Saccular Intracranial Aneurysms
A Prospective, Multi-center, Single Arm Study to Evaluate the Safety and Effectiveness of the CODMAN ENTERPRISE® Vascular Reconstruction Device and Delivery System When Used in Conjunction With Endovascular Coil Embolization in the Treatment of Wide-necked Saccular Intracranial Aneurysms
Enrollment Status: Terminated
Publish Date: October 23, 2020
Intervention Type: Device
Study Phase: Not Applicable
Stryker Neurovascular Trevo® Retriever Registry
Stryker Neurovascular Trevo® Retriever Registry
Enrollment Status: Completed
Publish Date: June 24, 2020
POSITIVE: PerfusiOn Imaging Selection of Ischemic STroke PatIents for EndoVascular ThErapy
POSITIVE: PerfusiOn Imaging Selection of Ischemic STroke PatIents for EndoVascular ThErapy
Enrollment Status: Terminated
Publish Date: November 13, 2019
Intervention Type: Device
Study Phase: Not Applicable
Diffusion Weighted Imaging (DWI) or Computerized Tomography Perfusion (CTP) Assessment With Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoing Neurointervention (DAWN)
Diffusion Weighted Imaging (DWI) or Computerized Tomography Perfusion (CTP) Assessment With Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoing Neurointervention (DAWN)
Enrollment Status: Completed
Publish Date: July 20, 2018
Intervention Type: Other, Device
Study Phase: Not Applicable
View 16 Less Clinical Trials

276 Total Publications

SUMMIT MAX: A randomized trial of the super large bore HiPoint Reperfusion System versus Vecta System for aspiration thrombectomy.
SUMMIT MAX: A randomized trial of the super large bore HiPoint Reperfusion System versus Vecta System for aspiration thrombectomy.
Journal: Stroke
Published: May 21, 2025
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Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

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