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NCT07508059 · ClinicalTrials.gov registry record · NA
High Resolution Pharyngeal Manometry (HRPM) Biofeedback
A NA study, sponsored by NYU Langone Health.
- Not yet
- Registry status
- NA
- Development phase
- 50
- Enrollment target
NCT07508059: Clinical Trial NA study, sponsored by NYU Langone Health.
NCT07508059 is a NA study that has not yet begun recruiting, run by NYU Langone Health. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07508059, a NA study, has not yet begun recruiting, sponsored by NYU Langone Health.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
Study Summary
The purpose of this study is to quantify the added benefit of visual biofeedback from High Resolution Pharyngeal Manometry (HRPM) for swallowing rehabilitation. Primary aims including assessing changes in swallowing biomechanics (pressure generation, timing) during swallow maneuvers with and without HRPM visual biofeedback. Secondary aim includes participant attitudes related to visual biofeedback and the experience of HRPM.
Primary Outcome
Pharyngeal contractile integral, a product of mean pharyngeal contractile amplitude, length, and duration. Low PhCI (\< 100-150 mmHg·s·cm): Indicates hypo-contractility or weakness while High PhCI (\> 200-300+ mmHg·s·cm): Represents stronger contraction strength
Interventions
- OTHER Swallowing Maneuvers
- DIAGNOSTIC_TEST High Resolution Pharyngeal Manometry (HRPM)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2026-05-01 |
| Est. Completion | 2027-05-01 |
| Phase | NA |
What is known before NCT07508059 opens enrollment
NCT07508059 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which Swallowing Maneuvers is the first listed.
NCT07508059 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07508059 about?
NCT07508059 is a clinical study titled "High Resolution Pharyngeal Manometry (HRPM) Biofeedback". The purpose of this study is to quantify the added benefit of visual biofeedback from High Resolution Pharyngeal Manometry (HRPM) for swallowing rehabilitation. Primary aims including assessing changes in swallowing biomechanics (pressure generation, timing) during swallow maneuvers with and without...
What is the current status of trial NCT07508059?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2026-05-01. Estimated completion is 2027-05-01.
What interventions are being tested in trial NCT07508059?
The interventions under investigation include: Swallowing Maneuvers (OTHER), High Resolution Pharyngeal Manometry (HRPM) (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT07508059?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07508059's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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