Feasibility Study to Evaluate Safety of Nutriseal™ Nutriplace™ System

Enteral Nutrition Clinical Trial

Official title:

A Feasibility Study to Evaluate the Clinical Safety of Nutriseal™ Enteral Feeding Tube Placement Using the Nutriseal™ Nutriplace™ System in Patients

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03371160
• Other study ID #: NUTRI001
• Status: Terminated
• Phase: N/A
• Start date: December 13, 2017
• Est. completion date: March 15, 2018

Study information

• Verified date: May 2024
• Source: Nutriseal L.P
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a single center, non-randomized feasibility clinical evaluation that is designed to affirm the safety of the Nutriplace™ System guidance during the placement of the Nutriseal™ enteral feeding tubes.

Description:

Enteral nutrition is the preferred route for the provision of nutritional support in most critical ill patients with functional gastrointestinal tract. Achieving early enteral nutrition (EN) in critically ill patients is associated with fewer major complications, reduced mortality and length of hospital stay, and significant cost savings.

It is estimated that approximately 1.2 million feeding tubes are placed blindly each year in the United States alone. Despite the obvious advantages of the enteral tube feeding, inadvertent placement of enteral feeding tube (EFT) into the airway is relatively common and can result in significant pulmonary injury including pneumothorax and pneumonia. Airway misplacement occurs in 1.2-4 % of blind EFT insertions, with 0.2 to 1.2% of all the feeding tube placements cause pulmonary complications to patients.

The gold standard for detecting inadvertent placement of a feeding tube in the lungs is radiography. However, because of its cost, possible delay of feedings while waiting for radiography, and risk for radiation exposure, clinicians continue to seek for alternative methods to confirm correct placement.

All the above mentioned, emphasizes the fact that safe and effective delivery of nasoenteral tube feedings requires assurance that the feeding tube tip is in a proper position.

The Nutriplace™ System is an electromagnetic tracking system which tracks the path of the feeding tube during placement.

The benefit of the system when EFT is misdirected into the pulmonary system is a real-time visual tracing, which may prompt users to withdraw the tube and reinsert it.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 22
• Est. completion date: March 15, 2018
• Est. primary completion date: March 15, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

1. Patients must be >21 years of age

2. Patients must require placement of a nasoenteral feeding tube

3. Patients have an endotracheal tube, OR Do not have an endotracheal tube but are sedated (RASS score of -2 or less) and/or obtunded (Glasgow Coma scale of 9-12)

4. Patients or legal authorized representative must be able to understand and adhere to all protocol procedures and be willing and able to provide written informed consent

Exclusion Criteria:

1. Patients must not have a history of:

• Esophageal varices or ulcers

• Upper airway obstruction

• Upper GI stenosis or obstruction

• Trauma involving sinuses, nares face or neck that would prevent Nasogastriv (NG) tube insertion

• Deformities of the sinus cavities and/or skull base

• Esophageal cancer or neoplasm

2. Patients must not have a significant concomitant illness that would adversely affect their participation in the study

3. Female patients who are pregnant or lactating

Related Conditions & MeSH terms

• Enteral Nutrition

Intervention

Device:
• Nutriplace™ System
The Nutriseal™ Nutriplace™ System is an electromagnetic tracking system for feeding tube placement designed to aid qualified operators in the placement of the Nutriseal™ Enteral Feeding Tube™ into the stomach or small intestine.

Locations

Country	Name	City	State
United States	Cleveland Clinic Foundation	Cleveland	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
Nutriseal L.P

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Successfully Placed Enteral Feeding Tube	Enteral tube (EFT) can be placed in the correct anatomical position without occurrence of guidance-related adverse events.; Procedure success was evaluated by comparing tube tip location according to the NUTRIPLACE System and abdominal and/or thoracic X-Ray.; Guidance-related AEs were evaluated through the documentation of any guidance-related serious adverse events (SAE) or adverse events (AE) occurring during a subject's participation in the study.	During procedure visit
Secondary	Number of Participants Requiring Replacement and/or Repositioning of the Feeding Tube	Number of placement attempts was evaluated by number of replacement and repositioning events, as defined below: Replacement: Complete removal of the tube from the patient or retraction above the level of the pharynx followed by reinsertion; Repositioning: Changing position of tube without complete removal of the tube	During procedure visit
Secondary	Number of Participants Reporting Retrograde Tube Migration in the Follow-up Visit	Tube Migration was defined as: Retrograde migration from desired placement position	During follow-up visit (20-48 hours post tube placement