A Clinical Study to Evaluate the Ultrasonic Detection of a Novel Nasogastric Tube in the Human Body.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNasotrak Medical Pte Ltd

About this trial

The purpose of this study is to evaluate the safety, efficacy and accuracy of the Nasotrak System in an adult patient population.

Eligibility criteria

Qualifiers

Adults greater than 18 years of age

Able to provide informed consent or have a legally authorized representative available to provide informed consent in English

Clinically requiring a 12 Fr NG/OG tube with X-ray confirmation per standard protocol

Disqualifiers

Female subjects of childbearing age with known pregnancy or lactating.

Prisoners.

Unable to consent in English.

Subjects/ volunteers with pacemakers or life-sustaining devices in the body such as ICD.

Trial design

Treatments tested in this trial

  • Nasotrak System

Treatment groups

90 Participants
are divided into 1 treatment group

Sponsors and collaborators