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Nasogastric/Orogastric Tube Placement Verification Study Using RightSpot pH Indicator to Verify Gastric Acidity

Evaluation of RightBio Metrics', RightSpot pH Indicator, for Rapid Bedside Verification of Proper Nasogastric/ Orogastric Tube Placement in Emergency Department & Intensive Care Unit Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01561729
Enrollment
30
Registered
2012-03-23
Start date
2012-01-31
Completion date
2014-12-31
Last updated
2014-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Small Bowel Obstruction, Gastrointestinal Hemorrhage

Keywords

nasogastric tube, orogastric tube, RightSpot pH Indicator, suction tube, RightBio Metrics, RightLevel, RightSpot Infant, NG Tube, pH, Gastric Acidity

Brief summary

This study will evaluate the use of RightBio Metrics' RightSpot device used to determine if there is proper placement of a nasogastric or orogastric tube.

Detailed description

Primary objective: To assess the level of accuracy of the RightSpot pH Indicator in determining correct placement of NG/OG tubes as compared to the gold standard of CXR in Emergency Department & ICU patients. Hypothesis 1: In greater than 90% of the cases, RightSpot pH Indicator will be successful in confirming the placement of NG/OG tubes by demonstrating a pH of 4.5 or less in patients with CXR proven tube placement. Hypothesis 2: The time to confirmation of NG/OG tube placement will be significantly less using the RightSpot pH Indicator than using CXR. The time will be calculated by the start time consisting of the time that the NG/OG tube was placed until the end time, which will be when the device pH Indicator testing is performed. The time to confirmation using the gold standard of a CXR will begin when the NG/OG tube is placed and end when the CXR is available on PACS (picture archiving and communication system). Secondary objective: To determine via subgroup analysis whether gross blood in the stomach, presence of acid-reducing medications, or trauma affects the accuracy of NG/OG placement determination by the RightSpot pH Indicator.

Interventions

DEVICERightSpot pH Indicator

The RightSpot pH Indicator device is used to confirm proper placement of all types of gastric tubes used for gastric rest, suction, or medicating/feeding by measuring the pH of stomach aspirate. This device is intended for 1 (one) SINGLE USE. The probability of proper placement is higher when the pH is less than or equal to 4.5 and if aspirate has a typical gastric fluid appearance (grassy green, brown, colorless- with possible shreds of off-white mucus or sediment).

Chest radiograph will be taken after tube placement to verify proper positioning of the nasogastric or orogastric tube.

Sponsors

RightBio Metrics
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients 18 years and older * Patient or proxy willing to provide informed consent * Patients who require placement of a nasogastric/orogastric tube, in the ED or ICU, as standard of care, AND a member of the study staff is available and present for NG/OG tube placement. * It is anticipated that the patient will remain in the ED/ICU in order to obtain RightSpot pH Indicator reading and verifying CXR

Exclusion criteria

* Patients less than 18 years of age * Patient or proxy unwilling or unable to provide informed consent * Patient with known or suspected pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Determination of proper placement of ng/og tubeParticipants will be followed until the determination of proper placement of the ng/og tube is made. This is anticipated to be less than 3 hours.The pH will be assessed by visual inspection of pH paper within the device. If the pH is noted to be less than 4.5 then the placement will be considered to be within the stomach.

Secondary

MeasureTime frameDescription
Confounding factors for using the RightSpot pH IndicatorParticipants will be followed until the determination of proper placement of the ng/og tube is made. This is anticipated to be less than 3 hours.A subgroup analysis will be done to determine whether gross blood in the stomach, presence of acid-reducing medications, or trauma affects the accuracy of NG/OG placement determination by the RightSpot pH Indicator.
Time to confirmation of tube placementParticipants will be followed until the determination of proper placement of the ng/og tube is made. This is anticipated to be less than 3 hours.The time to verification of tube placement will be measured for both chest radiograph and use of RightSpot pH Indicator.

Countries

United States

Contacts

Primary ContactJason Wilson, MD
tampaerdoc@gmail.com(813)627-5931

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026