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Safety and Efficacy Study of the FTRD System for Obtaining Full-thickness Intestinal Biopsies

NCT02673983 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2021-02-15

No results posted yet for this study

Summary

The aim of this study is to evaluate FTRD (full-thickness resection device) in terms of obtaining full-thickness biopsies form the gastrointestinal tract endoscopically in the work-up of patients with gastrointestinal motility disorders.

Conditions

  • Gastrointestinal Motility Disorders

Interventions

PROCEDURE

Endoscopic full-thickness biopsy

Sponsors & Collaborators

  • Region Skane

    lead OTHER

Principal Investigators

  • Henrik Thorlacius, MD, PhD · Region Skane, Department of Surgery

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-02-29
Primary Completion
2017-07-31
Completion
2017-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02673983 on ClinicalTrials.gov