- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07264322
Real-Time Dynamic Imaging Study of Normal Pharyngolaryngeal Structures During Barium Swallow (GLAM-III) (GLAM-III)
Observational Imaging Study on Real-Time Dynamic Changes of Normal Pharyngolaryngeal Structures During Barium Swallow in Patients Undergoing Routine Barium Meal Examination
Study Overview
Status
Conditions
Detailed Description
After approval by the Ethics Committee of Zhejiang Cancer Hospital (Approval Number: IRB-2025-1096(IIT)), this study will be registered on ClinicalTrials.gov prior to participant enrollment. Given that the study only utilizes de-identified imaging data from routine barium meal examinations (no additional procedures or interventions for participants), informed consent is exempted as approved by the Ethics Committee. The study is planned to be conducted from August 2025 to October 2025.
Eligible participants are patients undergoing routine barium meal examinations at Zhejiang Cancer Hospital, meeting the inclusion criteria (18-75 years old, no pharyngolaryngeal surgery/trauma/congenital malformation, no swallowing dysfunction, unobstructed oropharyngeal-esophageal pathway, etc.) and excluding those with contraindications (e.g., goiter compressing pharyngolaryngeal structures, barium allergy).
Barium Swallow Examination Procedure:
All procedures follow the standard clinical protocol for barium meal examinations, with no additional radiation exposure or burden on participants:
Static Imaging (Resting State): Participants assume a standing position. A digital X-ray machine (Shimadzu Uni-vision) is used to obtain static images of the pharyngolaryngeal region, recording the baseline anatomical positions of the pyriform sinus, cricoid cartilage lamina, and esophageal inlet.
Dynamic Imaging (Swallowing State): Participants are instructed to swallow 5ml, 10ml, 20ml, and 40ml of medical barium sulfate suspension (concentration: 160-200% W/V) sequentially. During swallowing, a dynamic fluoroscopic imaging system is activated (frame rate: 15 frames/second) to continuously record the entire process of barium passing from the oropharynx through the larynx to the esophagus (each swallowing event lasts approximately 5-10 seconds). Each participant repeats the swallowing action 4-5 times, and the clearest dynamic image sequence is selected for subsequent analysis.
Data Collection and Analysis:
Image analysis software is used for frame-by-frame parsing of dynamic images. Key anatomical structures (pyriform sinus boundaries, anterior edge of the cricoid cartilage lamina, esophageal inlet center) are labeled, and coordinate positioning technology is applied to analyze the following parameters:
Displacement and angle changes of pharyngolaryngeal structures from resting state to peak swallowing phase; Preferred pathway of barium through the oropharynx (unilateral pyriform sinus, bilateral pyriform sinuses, or central region of the cricoid cartilage lamina); Retention time of barium in the pyriform sinus and its passing speed; Expansion amplitude of the pyriform sinus and displacement distance of the cricoid cartilage lamina during swallowing
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Jiangling Wang, Ph. D
- Phone Number: +86 571 88122106
- Email: wangjl@zjcc.org.cn
Study Contact Backup
- Name: Xiaochun Jin, M.D
- Phone Number: +86 571 88122564
- Email: ec@zjcc.org.cn
Study Locations
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Zhejiang
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Hangzhou, Zhejiang, China, 310022
- Recruiting
- Jiangling Wang
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Principal Investigator:
- Jiangling Wang, Dr.
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Contact:
- Jiangling Wang, Dr.
- Phone Number: +8615168373331
- Email: wangjl@zjcc.org.cn
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Real-time dynamic changes of pharyngolaryngeal structures during swallowing
Time Frame: From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
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Measurement of displacement distance of the cricoid cartilage lamina, expansion amplitude of the pyriform sinus, and movement trajectory of the esophageal inlet during swallowing (assessed via dynamic fluoroscopic imaging).
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From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion of participants with consistent instrument insertion pathway and barium's preferred pathway (pyriform sinus)
Time Frame: From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
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Analysis of the consistency between the barium's preferred pathway (pyriform sinus) and the insertion pathway of laryngeal mask-related instruments, to explain the anatomical fit differences among three laryngeal mask designs (LMA Supreme, I-gel, GMA-Tulip).
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From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Barium flow speed through the oropharynx
Time Frame: From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
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The speed of barium flow through the oropharyngeal region, measured by videofluoroscopic swallowing study.
The speed will be calculated by tracking the movement of the barium bolus head between two predefined anatomical points (e.g., the pyriform sinus and the lower edge of the cricoid cartilage) and reported in millimeters per second (mm/s)
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From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
|
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Preferred pathway of barium flow
Time Frame: From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
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The primary anatomical pathway of the barium bolus as it passes the laryngeal inlet, assessed by videofluoroscopy.
The pathway will be categorized as either passing through the pyriform sinuses or through other channels (e.g., directly over the arytenoids).
The result will be reported as the proportion (percentage) of participants with barium flow primarily through the pyriform sinuses.
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From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
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Displacement of the cricoid cartilage lamina during barium swallow
Time Frame: From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
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The extent of posterior-inferior displacement of the cricoid cartilage lamina during the pharyngeal phase of swallowing, measured on lateral videofluoroscopic images.
The displacement will be quantified as the vertical distance (in millimeters) from the resting position of the cricoid cartilage to its maximum displaced position.
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From the initiation of the barium swallow to the complete passage of the bolus through the upper esophageal sphincter, as assessed under videofluoroscopy (an average of 15 minutes per participant).
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Pingbo Xu, Ph. D, Zhejiang Cancer Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB-2025-1096(IIT)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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