Thomas Walther
Expertise in
14
conditions

Thomas Walther

Frankfurt Am Main, HE, DE 
Expertise in
14
conditions
Frankfurt Am Main, HE, DE 
OverviewLocationsClinical Research

Overview

Thomas Walther practices in Frankfurt Am Main, Germany. Mr. Walther is highly rated in 14 conditions, according to our data. His top areas of expertise are Aortic Valve Stenosis, Aortic Regurgitation, Mitral Valve Regurgitation, Transcatheter Aortic Valve Replacement (TAVR), and Aortic Valve Replacement.

His clinical research consists of co-authoring 470 peer reviewed articles and participating in 11 clinical trials. MediFind looks at clinical research from the past 15 years.

Gender
Male

Locations

Frankfurt Am Main, HE 60596, Germany
Other Locations
Dresden, SN 01069, Germany
Berlin, BE 14197, Germany
Darmstadt, HE 64289, Germany
St. Franziskus Hospital, Siegburg, NW, Germany
Greifswald, MV 17489, Germany
Rhein, NW, Germany
Hessen, ST, Germany
Hamburg, HH, Germany
Luebeck, SH, Germany
Bochum, NW 44801, Germany
Leipzig, SN 04347, Germany
Heidelberg, BW, Germany
Nauheim, HE, Germany
Bad Nauheim, HE, Germany
Koeln, NW, Germany
Mannheim, BW, Germany
Germany
Bad, BY, Germany
Bernried, 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.

10 Clinical Trials

Expanded Clinical Study of the Tendyne Mitral Valve System
Expanded Clinical Study of the Tendyne Mitral Valve System
Enrollment Status: Completed
Publish Date: July 17, 2025
Intervention Type: Device
Study Phase: Not Applicable
Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitation (RESOLVE-MR) (Tendyne™ PMCF Study)
Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitation (RESOLVE-MR) (Tendyne™ PMCF Study)
Enrollment Status: Active_not_recruiting
Publish Date: June 12, 2024
Intervention Type: Device
Randomized, Multi-Center, Event-Driven Trial of TAVI Versus SAVR in Patients With Symptomatic Severe Aortic Valve Stenosis and Intermediate Risk of Mortality, as Assessed by STS-Score - DEDICATE
Randomized, Multi-Center, Event-Driven Trial of TAVI Versus SAVR in Patients With Symptomatic Severe Aortic Valve Stenosis and Intermediate Risk of Mortality, as Assessed by STS-Score - DEDICATE
Enrollment Status: Active_not_recruiting
Publish Date: April 26, 2024
Intervention Type: Device, Procedure
Study Phase: Not Applicable
Beating Heart Mitral Valve REPair With the HARPOON™ System: ReaL World Outcomes From a multICenter observATional European Registry
Beating Heart Mitral Valve REPair With the HARPOON™ System: ReaL World Outcomes From a multICenter observATional European Registry
Enrollment Status: Terminated
Publish Date: January 29, 2024
Intervention Type: Device
Study Phase: Not Applicable
Assessment of the Safety and Performance of the HARPOON™ Beating Heart Mitral Valve Repair System; a Multi-center Post-market Study (ASCEND)
Assessment of the Safety and Performance of the HARPOON™ Beating Heart Mitral Valve Repair System; a Multi-center Post-market Study (ASCEND)
Enrollment Status: Terminated
Publish Date: December 22, 2023
Intervention Type: Device
Study Phase: Not Applicable
Operative Mitralklappenrekonstruktion Bei Funktionellen Mitralklappenvitien Bei Reduzierter Systolischer Ventrikelfunktion
Operative Mitralklappenrekonstruktion Bei Funktionellen Mitralklappenvitien Bei Reduzierter Systolischer Ventrikelfunktion
Enrollment Status: Completed
Publish Date: September 28, 2023
Intervention Type: Procedure
ACURATE Neo™ Aortic Bioprosthesis for Implantation Using the ACURATE TA™ LP Transapical Delivery System in Patients With Severe Aortic Stenosis
ACURATE Neo™ Aortic Bioprosthesis for Implantation Using the ACURATE TA™ LP Transapical Delivery System in Patients With Severe Aortic Stenosis
Enrollment Status: Completed
Publish Date: April 09, 2020
Intervention Type: Device
Study Phase: Not Applicable
Safety and Performance Study of the Edwards SAPIEN 3 Transcatheter Heart Valve
Safety and Performance Study of the Edwards SAPIEN 3 Transcatheter Heart Valve
Enrollment Status: Completed
Publish Date: April 01, 2020
Intervention Type: Device
Study Phase: Not Applicable
A Randomized, Parallel Group, Double-Blind Study of Ticagrelor Compared With Aspirin for Prevention of Vascular Events in Patients Undergoing Coronary Artery Bypass Graft Operation TiCAB- Ticagrelor in CABG
A Randomized, Parallel Group, Double-Blind Study of Ticagrelor Compared With Aspirin for Prevention of Vascular Events in Patients Undergoing Coronary Artery Bypass Graft Operation TiCAB- Ticagrelor in CABG
Enrollment Status: Terminated
Publish Date: August 02, 2018
Intervention Type: Drug
Study Phase: Phase 3
The RELIEF Trial: REduction or eLimination of mItral rEgurgitation in Degenerative or Functional Mitral Regurgitation With the CardiAQ-Edwards™ Transcatheter Mitral Valve
The RELIEF Trial: REduction or eLimination of mItral rEgurgitation in Degenerative or Functional Mitral Regurgitation With the CardiAQ-Edwards™ Transcatheter Mitral Valve
Enrollment Status: Withdrawn
Publish Date: January 09, 2018
Intervention Type: Device
Study Phase: Phase 1/Phase 2
View 9 Less Clinical Trials

470 Total Publications

The Performance of Commercial pH-Sensitive Ion-Selective Field Effect Transistors.
The Performance of Commercial pH-Sensitive Ion-Selective Field Effect Transistors.
Journal: ChemistryOpen
Published: June 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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