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NOT YET RECRUITING
NCT06468800
NA

Feasibility and Added Value of the TRACMOTION Device for ESD

Sponsor: Erasmus Medical Center

View on ClinicalTrials.gov

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

Interventions

DEVICE

TRACMOTION

Patients already scheduled for ESD will undergo an ESD procedure with the aid of the Tracmotion device