Advanced in Thoracic Aortic Aneurysm

Dierk Scheinert

Leipzig, SN, DE 
Advanced in Thoracic Aortic Aneurysm
Leipzig, SN, DE 
OverviewLocationsClinical Research

Overview

Dierk Scheinert practices in Leipzig, Germany. Mr. Scheinert is rated as an Advanced expert by MediFind in the treatment of Thoracic Aortic Aneurysm. His top areas of expertise are Peripheral Artery Disease, Atherosclerosis, SVC Obstruction, Angioplasty, and Stent Placement.

His clinical research consists of co-authoring 183 peer reviewed articles and participating in 17 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 25 articles and participated in 1 clinical trial in the study of Thoracic Aortic Aneurysm.

Gender
Male

Locations

Leipzig, SN 04103, Germany
Other Locations
Jena, TH 07747, Germany
Bad Bevensen, NI, Germany
Universitäts Herzzentrum Freiburg Bad Krozingen
Bad Krozingen, BW, Germany
Frankfurt Am Main, HE, Germany
Rosenheim, BY, Germany
Erlangen, BY, Germany

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts 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

Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registry
Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registry
Enrollment Status: Active_not_recruiting
Publish Date: October 10, 2025
Intervention Type: Procedure, Device
Stellarex Vascular E-Registry
Stellarex Vascular E-Registry
Enrollment Status: Completed
Publish Date: August 14, 2025
Intervention Type: Device
PQ Bypass Systems for Femoropopliteal Bypass II (PQB 4 FP II)
PQ Bypass Systems for Femoropopliteal Bypass II (PQB 4 FP II)
Enrollment Status: Completed
Publish Date: May 23, 2025
Intervention Type: Device
Study Phase: Not Applicable
The Detour Endovascular Technique for Long OcclUsive Fem-pop Revascularization - 2 Clinical Trial
The Detour Endovascular Technique for Long OcclUsive Fem-pop Revascularization - 2 Clinical Trial
Enrollment Status: Completed
Publish Date: April 02, 2025
Intervention Type: Device
Study Phase: Not Applicable
Randomized & Controlled Noninferiority Trial to Evaluate Safety & Clinical Efficacy of SurVeil™ Drug-Coated Balloon (DCB) iN Treatment of Subjects With Stenotic Lesions of Femoropopliteal Artery Compared to Medtronic IN.PACT® Admiral® DCB
Randomized & Controlled Noninferiority Trial to Evaluate Safety & Clinical Efficacy of SurVeil™ Drug-Coated Balloon (DCB) iN Treatment of Subjects With Stenotic Lesions of Femoropopliteal Artery Compared to Medtronic IN.PACT® Admiral® DCB
Enrollment Status: Completed
Publish Date: March 25, 2025
Intervention Type: Device
Study Phase: Not Applicable
BEST SFA Pilot Study - Best Endovascular STrategy for Complex Lesions of the Superficial Femoral Artery Comparing a Stent-avoiding (study Arm) Versus Stent-preferred (control Arm) Approach Within a Prospective, Randomized, Multi-center Trial
BEST SFA Pilot Study - Best Endovascular STrategy for Complex Lesions of the Superficial Femoral Artery Comparing a Stent-avoiding (study Arm) Versus Stent-preferred (control Arm) Approach Within a Prospective, Randomized, Multi-center Trial
Enrollment Status: Active_not_recruiting
Publish Date: December 09, 2024
Intervention Type: Device
Study Phase: Not Applicable
Randomized Study of the Shockwave Medical Peripheral Lithoplasty® System Used in Combination With DCB Versus Standard Balloon Angioplasty Used in Combination With DCB to Treat Moderate and Severely Calcified Femoropopliteal Arteries
Randomized Study of the Shockwave Medical Peripheral Lithoplasty® System Used in Combination With DCB Versus Standard Balloon Angioplasty Used in Combination With DCB to Treat Moderate and Severely Calcified Femoropopliteal Arteries
Enrollment Status: Completed
Publish Date: December 20, 2023
Intervention Type: Device, Drug
Study Phase: Not Applicable
Prospective, Randomized, Multi-Center Study for the Treatment of Subjects With Symptomatic Femoropopliteal Artery Disease With the Ranger Paclitaxel Coated PTA Balloon Catheter (Study Arm) Versus the IN.PACT Drug Eluting Balloon (Control Arm)
Prospective, Randomized, Multi-Center Study for the Treatment of Subjects With Symptomatic Femoropopliteal Artery Disease With the Ranger Paclitaxel Coated PTA Balloon Catheter (Study Arm) Versus the IN.PACT Drug Eluting Balloon (Control Arm)
Enrollment Status: Completed
Publish Date: December 20, 2023
Intervention Type: Device
Study Phase: Not Applicable
A Non-randomized Trial of the Temporary Spur Stent System for the Treatment of Lesions Located in the Infrapopliteal Arteries Outside of the United States
A Non-randomized Trial of the Temporary Spur Stent System for the Treatment of Lesions Located in the Infrapopliteal Arteries Outside of the United States
Enrollment Status: Active_not_recruiting
Publish Date: November 18, 2023
Intervention Type: Device
Study Phase: Not Applicable
A Randomized Trial to Confirm the Safety and Effectiveness of Chocolate Touch™ Paclitaxel Coated Balloon Catheter, in Above the Knee Lesions
A Randomized Trial to Confirm the Safety and Effectiveness of Chocolate Touch™ Paclitaxel Coated Balloon Catheter, in Above the Knee Lesions
Enrollment Status: Active_not_recruiting
Publish Date: October 30, 2023
Intervention Type: Device
Study Phase: Not Applicable
Clinical Investigation Plan (CIP) for Safety and Performance Study of Large Hole Vascular Closure Device - FRONTIER IV Study
Clinical Investigation Plan (CIP) for Safety and Performance Study of Large Hole Vascular Closure Device - FRONTIER IV Study
Enrollment Status: Completed
Publish Date: February 01, 2023
Intervention Type: Device
Study Phase: Not Applicable
A Prospective, Multicenter, Single Blind, Randomized, Controlled Trial Comparing the Lutonix Drug Coated Balloon Versus Standard Balloon Angioplasty for Treatment of Below-the-Knee (BTK) Arteries(Lutonix BTK Trial)
A Prospective, Multicenter, Single Blind, Randomized, Controlled Trial Comparing the Lutonix Drug Coated Balloon Versus Standard Balloon Angioplasty for Treatment of Below-the-Knee (BTK) Arteries(Lutonix BTK Trial)
Enrollment Status: Completed
Publish Date: February 09, 2022
Intervention Type: Device
Study Phase: Not Applicable
DESappear Study: Drug Eluting Scaffold With an Absorbable Platform for Primary Lower Extremity Arterial Revascularization
DESappear Study: Drug Eluting Scaffold With an Absorbable Platform for Primary Lower Extremity Arterial Revascularization
Enrollment Status: Completed
Publish Date: June 01, 2021
Intervention Type: Device
Study Phase: Not Applicable
A Prospective, Multicenter, Single Arm Real-World Registry Investigating the Clinical Use and Safety of the Lutonix Drug Coated Balloon Percutaneous Transluminal Angioplasty (PTA) Catheter for Treatment of Below-the-Knee (BTK) Arteries
A Prospective, Multicenter, Single Arm Real-World Registry Investigating the Clinical Use and Safety of the Lutonix Drug Coated Balloon Percutaneous Transluminal Angioplasty (PTA) Catheter for Treatment of Below-the-Knee (BTK) Arteries
Enrollment Status: Completed
Publish Date: January 13, 2020
Intervention Type: Device
An Evaluation of the 480 Biomedical STANZA™ Drug-Eluting Resorbable Scaffold (DRS) System in the Treatment of de Novo SFA Lesions
An Evaluation of the 480 Biomedical STANZA™ Drug-Eluting Resorbable Scaffold (DRS) System in the Treatment of de Novo SFA Lesions
Enrollment Status: Completed
Publish Date: September 06, 2019
Intervention Type: Device
Study Phase: Not Applicable
A Single-Arm, Multicenter Study for the Lower Extremities Using the Vanguard IEP Peripheral Balloon Angioplasty System With Integrated Embolic Protection
A Single-Arm, Multicenter Study for the Lower Extremities Using the Vanguard IEP Peripheral Balloon Angioplasty System With Integrated Embolic Protection
Enrollment Status: Completed
Publish Date: July 10, 2019
Intervention Type: Device
Study Phase: Not Applicable
Clinical Investigation Plan (CIP) for Safety and Performance Study of Large Hole Vascular Closure Device - FRONTIER III Study
Clinical Investigation Plan (CIP) for Safety and Performance Study of Large Hole Vascular Closure Device - FRONTIER III Study
Enrollment Status: Completed
Publish Date: February 01, 2018
Intervention Type: Device
Study Phase: Not Applicable
View 16 Less Clinical Trials

183 Total Publications

Outcomes at Patient and Limb Levels in Peripheral Artery Disease by the Location of Atherosclerotic Lower Limb Lesions: An Observational Study from a High-Volume German Center.
Outcomes at Patient and Limb Levels in Peripheral Artery Disease by the Location of Atherosclerotic Lower Limb Lesions: An Observational Study from a High-Volume German Center.
Journal: Journal of clinical medicine
Published: August 24, 2025

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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