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Feasibility and Added Value of the TRACMOTION Device for ESD
Sponsor: Erasmus Medical Center
Summary
A single center non-randomized prospective clinical study, to evaluate the feasibility and added value of the CE-certified Tracmotion device in patients scheduled consecutively for ESD in the upper and lower gastrointestinal tract. After ESD, the endoscopists' opinion will be evaluated with a short questionnaire on experience with the Tracmotion device. The pathology report will be checked for radicality and microscopic damage of the removed lesion.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
20
Start Date
2024-10-01
Completion Date
2025-03-01
Last Updated
2024-08-28
Healthy Volunteers
No
Conditions
Interventions
TRACMOTION
Patients already scheduled for ESD will undergo an ESD procedure with the aid of the Tracmotion device