Clinical trial Recruiting at 1 site Observational Ages 18 to 75

Real-time imaging of normal throat and larynx motion during a barium swallow

Official title: Observational Imaging Study on Real-Time Dynamic Changes of Normal Pharyngolaryngeal Structures During Barium Swallow in Patients Undergoing Routine Barium Meal Examination

Run by Zhejiang Cancer Hospital · NCT07264322 · Data updated 2026-11-12

This project will record routine barium-swallow X-rays to see how normal throat and voice-box structures move in adults.

Quick facts

Study typeObservational
Ages18 Years to 75 Years
SexAll
Enrollment3 (estimated)
SponsorZhejiang Cancer Hospital
Academic / other
Drugs / interventionsradiation
Locations1 site (Hangzhou, Zhejiang)
StatusRecruiting
StartedSeptember 10, 2025
Main results expectedDecember 30, 2025
Study endsDecember 30, 2025
Registry record updatedDecember 4, 2025
Trial IDNCT07264322 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–75 who are already scheduled for a routine barium meal exam and have normal pharyngolaryngeal anatomy and no swallowing dysfunction are ideal candidates.

Probably not a fit

People with prior pharyngolaryngeal surgery, anatomical abnormalities, compressive lesions, swallowing disorders, or barium allergy are unlikely to benefit from this imaging-only project.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational project uses de-identified images from routine barium meal examinations at Zhejiang Cancer Hospital to capture both static and real-time dynamic views of the pharyngolaryngeal region. Participants will undergo standard clinical static imaging at rest and dynamic imaging while swallowing measured volumes of barium (5, 10, 20, 40 ml) with a digital X-ray system. Only patients aged 18–75 with normal pharyngolaryngeal anatomy and unobstructed swallowing will be included, and no extra procedures or radiation beyond standard care are required. The recorded movement patterns will be analyzed to provide anatomical and physiological data relevant to laryngeal mask design and fit.

Why it matters

Potential benefit: If successful, the findings could help improve the anatomical fit and safety of laryngeal masks used for airway management.

How similar studies have gone: Fluoroscopic and videofluoroscopic swallowing studies are well-established for characterizing swallowing mechanics, but using those measurements specifically to guide laryngeal mask design is a relatively novel application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Aged 18-75 years;
* No history of pharyngolaryngeal surgery, trauma, or congenital malformation;
* No swallowing dysfunction, pharyngolaryngeal inflammation, or neurological diseases affecting swallowing;
* No recent use of drugs that affect muscle function (e.g., muscle relaxants, anticholinergics);
* Barium meal examination confirms unobstructed oropharyngeal-esophageal pathway;
* Normal pharyngolaryngeal anatomical structure (confirmed by preliminary imaging review);
* Scheduled to undergo routine barium meal examination at Zhejiang Cancer Hospital for clinical diagnosis.

Exclusion Criteria:

* Presence of diseases that may compress pharyngolaryngeal structures (e.g., goiter, mediastinal mass);
* Allergy to barium sulfate or other components of the barium suspension.

Where it's running

  • Jiangling Wang
    Hangzhou, Zhejiang, China
    Recruiting

Study contacts

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.