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Clinical Evaluation of the VIPUN Balloon Catheter 0.2 in Critically Ill Patients

NCT03512145 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2019-09-03

No results posted yet for this study

Summary

An open label, non-randomized, monocentric, interventional investigation in a cohort of adult critically ill patients

Conditions

  • Critical Illness
  • Intolerance; Nutritional
  • Delayed Gastric Emptying
  • Gastric Motor Dysfunction

Interventions

DEVICE

VIPUN Balloon Catheter

Gastric motility is recorded continuously with the VIPUN Balloon Catheter for 10 hours.

Sponsors & Collaborators

  • Prof Dr Jan Tack

    lead OTHER

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-04-16
Primary Completion
2019-08-01
Completion
2019-08-30

Countries

  • Belgium

Study Locations

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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 NCT03512145 on ClinicalTrials.gov