Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Mechanisms Preventing Pharyngeal Reflux

NCT05696184 · View on ClinicalTrials.gov ↗

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

614 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05696184

The ClinicalTrials.gov registry entry for NCT05696184 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medical College of Wisconsin, which has 614 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05696184 reports 1 study location spanning 1 distinct geographic area — top geographies include Wisconsin. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

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). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05696184?

This trial is sponsored by Medical College of Wisconsin, which has 614 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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