Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02430571 · ClinicalTrials.gov registry record

Case Series to Evaluate the Identification of Anatomical Markers Using the KANGAROO™ Feeding Tube

A clinical trial, sponsored by Medtronic - MITG.

Completed
Registry status
49
Enrollment target

NCT02430571: Completed study, sponsored by Medtronic - MITG.

NCT02430571 is a clinical trial that has completed, run by Medtronic - MITG. The registered enrollment target is 49 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02430571 has completed, sponsored by Medtronic - MITG.

COMPLETED
Registry status
49 participants
Enrollment target

Study Summary

This is a prospective, single-center, open label, within-subject clinical trial to evaluate the identification of anatomical markers in the gastrointestinal tract using the IRIS feeding tube. The trial will evaluate hospitalized subjects who require short-term enteral feeding with an anticipated duration of at least 3 days while in an intensive care unit (ICU) or step-down unit. Eligible men and women at least 18 years of age who give voluntary, written informed consent to participate in the clinical investigation will be included as subjects. If a potential subject is incapacitated and unable to provide informed consent, a designated legally authorized representative will be allowed to provide the informed consent on behalf of the subject to allow their participation in the study. Study entry will be defined as the point of signed informed consent. A Prospective, Single-Center, Open Label, Within-Subject Case Series to Evaluate the Identification of Anatomical Markers in the Gastrointestinal Tract Using the KANGAROO™ Feeding Tube with IRIS Technology

Primary Outcome

the following anatomical structures will be noted if visualized and the depth of feeding tube will also be recorded corresponding to the visualized structure: trachea/carina, esophagus, stomach

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2015-04
Est. Completion 2016-09
Medtronic - MITG

119 total trials

What the finished NCT02430571 record still lists

NCT02430571 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 49 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT02430571 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02430571 about?

NCT02430571 is a clinical study titled "Case Series to Evaluate the Identification of Anatomical Markers Using the KANGAROO™ Feeding Tube". This is a prospective, single-center, open label, within-subject clinical trial to evaluate the identification of anatomical markers in the gastrointestinal tract using the IRIS feeding tube. The trial will evaluate hospitalized subjects who require short-term enteral feeding with an anticipated dur...

What is the current status of trial NCT02430571?

This trial is currently completed. The enrollment target is 49 participants. The study started on 2015-04. Estimated completion is 2016-09.

Who is sponsoring clinical trial NCT02430571?

This trial is sponsored by Medtronic - MITG, which has 119 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02704858 · 49 participants · Phase 1

    Safety and Efficacy Study in Recurrent or Progressive Grade III or IV IDH1 Mutated Glioma

  • NCT03516708 · 49 participants · Phase 1

    Epacadostat (INCB024360) Added to Preoperative Chemoradiation in Patients With Locally Advanced Rectal Cancer

  • NCT03692429 · 49 participants · Phase 1

    alloSHRINK - Standard cHemotherapy Regimen and Immunotherapy With Allogeneic NKG2D-based CYAD-101 Chimeric Antigen Receptor T-cells

  • NCT04329494 · 49 participants · Phase 1

    PIPAC for the Treatment of Peritoneal Carcinomatosis in Patients With Ovarian, Uterine, Appendiceal, Colorectal, or Gastric Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02430571, the US trial registry maintained by the National Library of Medicine. NCT02430571 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.