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NCT05696184 · ClinicalTrials.gov registry record · NA

Mechanisms Preventing Pharyngeal Reflux

A NA study of GERD, sponsored by Medical College of Wisconsin.

Recruiting
Registry status
NA
Development phase
300
Enrollment target
1
Study location

NCT05696184 is a NA study of GERD that is actively recruiting participants, run by Medical College of Wisconsin. The registered enrollment target is 300 participants, above the 148-participant average among 15 other GERD trials with a reported enrollment target (103% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT05696184, a NA study of GERD, is actively recruiting participants, sponsored by Medical College of Wisconsin.

RECRUITING
Registry status
NA
Development phase
300 participants
Enrollment target
1
Study location

Study Summary

The overall goal is to define and characterize the manometric characteristics of UES incompetence associated with objectively documented pharyngeal reflux. The investigators will use endoscopic reflux detection as gold standard.

Conditions Studied

Interventions

  • DIAGNOSTIC_TEST Concurrent manometry/impedance/pH with video pharyngo-laryngoscopy
  • DIAGNOSTIC_TEST Slow and rapid intra-esophageal infusion

Study Locations (1)

Wisconsin

  • Medical College of Wisconsin - Milwaukee

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2013-11-01
Est. Completion 2026-10-12
Phase NA

Sponsor

Medical College of Wisconsin

447 total trials

What the Registry Record Tells You About NCT05696184

The ClinicalTrials.gov registry entry for NCT05696184 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 148-participant average among 15 other GERD trials with a reported enrollment target (103% higher). The listed sponsor is Medical College of Wisconsin, which has 447 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with GERD appearing as the primary indexed condition, and to 2 interventions - of which Concurrent manometry/impedance/pH with video pharyngo-laryngoscopy is the first listed.

NCT05696184 reports 1 study location spanning 1 distinct geographic area - top geographies include Wisconsin.

Frequently Asked Questions

What is clinical trial NCT05696184 about?

NCT05696184 is a clinical study titled "Mechanisms Preventing Pharyngeal Reflux". The overall goal is to define and characterize the manometric characteristics of UES incompetence associated with objectively documented pharyngeal reflux. The investigators will use endoscopic reflux detection as gold standard.

What is the current status of trial NCT05696184?

This trial is currently recruiting. It is a NA study. The enrollment target is 300 participants. The study started on 2013-11-01. Estimated completion is 2026-10-12.

What conditions does trial NCT05696184 study?

This clinical trial studies the following conditions: GERD.

What interventions are being tested in trial NCT05696184?

The interventions under investigation include: Concurrent manometry/impedance/pH with video pharyngo-laryngoscopy (DIAGNOSTIC_TEST), Slow and rapid intra-esophageal infusion (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT05696184?

This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05696184 being conducted?

This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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