Brief Title
Use of Virtual Reality for Procedural Planning of Transcatheter Aortic Valve Replacement
Official Title
Use of Virtual Reality for Procedural Planning of Transcatheter Aortic Valve Replacement (TAVR)
Brief Summary
This study sought to evaluate the impact of Virtual Reality (VR) tools in procedural planning of transcatheter aortic valve replacement (TAVR).
Detailed Description
A prospective study involving 11 patients referred for TAVR was conducted. A multidetector computed tomography (MDCT) was used to acquire and segment the anatomy of the access route and landing zone. From the information obtained with the MDCT in DICOM format, the investigators built a virtual platform (VisuaMed, Teacher Team. Valencia. Spain) that contains all the clinical information of the patients and a virtualized model of their anatomy. Wearing VR devices, the professional was able to "walk inside " the anatomy in an interactive and immersive way. Decisions after the evaluation of routine clinical images were compared with those after experience with VR models and intraprocedural findings.
Study Type
Interventional
Primary Outcome
TAVR procedure planning (prosthesis size, implant technique requirements, potential risks)
Condition
Aortic Stenosis, Severe
Intervention
TAVR planning
Study Arms / Comparison Groups
TAVR standard
Description: TAVR planning evaluated without VR and TAVR planning after VR analysis
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Recruitment Status
Diagnostic Test
Estimated Enrollment
11
Start Date
May 1, 2020
Completion Date
May 31, 2021
Primary Completion Date
May 31, 2021
Eligibility Criteria
Inclusion Criteria: - Severe aortic stenosis considered for TAVR procedure at a single Institution Exclusion Criteria: - None
Gender
All
Ages
N/A - N/A
Accepts Healthy Volunteers
No
Contacts
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Location Countries
Spain
Location Countries
Spain
Administrative Informations
NCT ID
NCT04944667
Organization ID
Cardiac Surgery CentroMT
Responsible Party
Principal Investigator
Study Sponsor
Centro Medico Teknon
Collaborators
Techer Team SL. Valencia. Spain
Study Sponsor
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Verification Date
March 2022