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WithdrawnNCT01308502Updated Mar 30, 2012

A New Nasopharyngeal pH Probe for Diagnosis of Laryngopharyngeal Reflux

A Phase 4 interventional study of Dx-pH probe in Laryngopharyngeal Reflux, sponsored by Children's Hospital of Philadelphia. Withdrawn at 1 site in United States. Open to participants aged 1 Month to 17 Years. Per ClinicalTrials.gov, last updated 2012-03-30.

Sponsored by Children's Hospital of Philadelphia · Phase 4, Interventional, and Diagnostic

Why this study was withdrawn
Difficulty recruiting patients due to logistics
Phase
Phase 4
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
1 Month to 17 Years
Sex
All
01

Study summary

The purpose of this study is to evaluate the utility of a minimally invasive nasopharyngeal pH probe for the diagnosis of laryngopharyngeal reflux (LPR) in children with airway compromise; to determine whether it is comparable to the gold standard esophageal pH probe in identifying LPR in this population; and to correlate results of pH testing with validated questionnaires. Our hypothesis is that a nasopharyngeal pH probe is equivalent to an esophageal probe in identifying laryngopharyngeal reflux.

Read the detailed description

Laryngopharyngeal reflux (LPR) has been repeatedly linked to upper respiratory symptoms in the pediatric population. Children with LPR may present with laryngomalacia, subglottic stenosis, laryngitis, and vocal cord nodules among other illnesses. Pharyngeal reflux has even been implicated in causing common childhood illnesses such as sinusitis and otitis media. Diagnosing LPR can be difficult, especially in children. Often otolaryngologists depend on a general gestalt to diagnosis LPR. In some cases, physicians rely on a Reflux Symptoms Index (RSI) questionnaire filled out by the caretaker and/or a Reflux Finding Score (RFS) filled out by the practitioner. Others have attempted to use a variety of tools to measure pH in the upper airway and proximal esophagus.

Initial research focused on correlating gastroesophageal reflux (GER) with otolaryngologic illnesses. These studies relied mostly on esophageal pH probes placed at the lower esophageal sphincter. With the realization that extraesophageal reflux or LPR was a separate disease, new methods have developed to quantify it. The dual esophageal pH probe is the current gold standard for measuring LPR as it records pH just above the proximal esophageal sphincter. Conditions such as chronic pediatric sinusitis, otitis media, laryngitis and globus are believed to arise from laryngopharyngeal reflux. Unfortunately, this device fails to identify many patients with LPR who would benefit from treatment, and radiographic studies are limited by their short duration of evaluation and risk of radiation. In addition, the placement of the esophageal pH probe is relatively invasive requiring both sedation and x-rays to confirm placement. Finally, they are difficult to place and maintain in children, necessitating a hospital stay for 24 hours while data is collected. The alternative is empiric treatment with Histamine 2 blockers and/or Protein Pump Inhibitors for an extended course, which has been shown to improve symptoms in many of these patients but is not without risk.

The new Dx-pH nasopharyngeal probe is the only tool available for directly measuring nasopharyngeal pH. It is an exempted class I medical device and is Food and Drug Administration (FDA)-approved for general use in the population. The device, manufactured by Respiratory Technology Corporation ISO (ResTech), measures the pH of both liquid and aerosolized droplets. It is positioned posterior to the soft palate and placement is confirmed by visualizing the light-emitting diode (LED) at the tip of the device. It is significantly less invasive than esophageal pH probes, does not require general anesthesia for placement, and can be used in an outpatient setting.

The Dx-pH probe is currently being used clinically in adult and pediatric practices to diagnose and monitor laryngopharyngeal reflux with only limited research supporting its use. A literature review finds only 6 studies that address the Dx-pH probe, of which, only 1 pilot study has been performed in children. This study looked at changes in pH in the trachea of 3 children with chronic tracheostomies. However, to date, no research has been published on the utility of the probe in diagnosing LPR in children. The probe, if effective, would be a valuable tool for diagnosing LPR in the pediatric population because of its limited risk and potential ability to replace more invasive and costly procedures.

02

Conditions studied

  • Laryngopharyngeal Reflux

Keywords

  • laryngopharyngeal reflux
  • LPR
  • GERD
  • gastroesophageal reflux
  • nasopharyngeal probe
03

In context

Gastroesophageal Reflux

1,066 studies on the registry are indexed under Gastroesophageal Reflux; 188 are open to participants now.

Browse Gastroesophageal Reflux studies →

Lead sponsor

Children's Hospital of Philadelphia is the lead sponsor of 480 studies on the registry; 85 are open to participants now.

Of its 28 completed or terminated interventional studies of FDA-regulated products, 22 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Month to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • History of airway compromise
  • Undergoing microlaryngoscopy, bronchoscopy, esophagoscopy, and esophageal pH probe placement at CHOP

Exclusion criteria

Exclusion Criteria:

  • Patients not undergoing esophageal pH probe placement
  • Neonates under 1 month of age
  • Adults over 18 years of age or older.
05

Study design

Phase
Phase 4
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Probe

    Children with airway obstruction

    Device: Dx-pH probe

Interventions

  • DeviceDx-pH probe

    Dx-pH probe with 24 hour recording

    Also known as: ResTech Dx-pH probe

06

What researchers measure

Primary outcomes

  1. nasopharyngeal pH

    Change in nasopharyngeal pH as measured by the Dx-pH probe

    Time frame: 24 hours

07

Study locations

1 site
  • Children's Hospital of Philadelphia
    Philadelphia, Pennsylvania 19104, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01308502
Lead sponsor
Children's Hospital of Philadelphia
Responsible party
Karen Zur (Associate Director, The Center for Pediatric Airway Disorders, Director Pediatric Voice Program, Children's Hospital of Philadelphia) — Principal investigator
First posted
Mar 4, 2011
Start date
Jan 2010
Primary completion
Jan 2012 (estimated)
Completion
Jan 2012 (estimated)
Last update
Mar 30, 2012

Study contacts

Karen Zur
principal investigator · Children's Hospital of Philadelphia

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Mar 2012. You cannot join it, but the record below documents what was studied.

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