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NCT Number: NCT07594561

Normative Swallowing Physiological Metrics of Pharyngeal High-Resolution Impedance Manometry in Chinese Adults

As Taiwan enters a super-aged society in 2025, the number of elderly patients and patients with multiple comorbidities continues to increase, and the risk of dysphagia rises with advancing age. Due to neuronal degeneration and muscle atrophy, older adults often experience delayed recovery of swallowing function after general anesthesia, and it may take up to seven days to regain their baseline swallowing ability. Therefore, postoperative monitoring of swallowing function and early rehabilitative intervention are crucial for reducing complication risks and facilitating early discharge.

Currently, there is limited literature regarding normative data for pharyngeal swallowing assessment using high-resolution pharyngeal manometry with impedance as well as videofluoroscopic swallowing studies in the Chinese population. This project aims to recruit 80 healthy adults to establish normative reference values.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Observational

About this study

To ensure relative consistency in the physiological, pathological, and psychological conditions of participants, this study will recruit 80 healthy adults without swallowing difficulties using convenience sampling from outpatient clinics and the general healthy population at National Taiwan University Hospital (NTUH). All participants will undergo both videofluoroscopic swallowing study (VFSS) and high-resolution pharyngeal manometry with impedance (HRIM). Inclusion criteria include adults aged ≥18 years without subjective dysphagia. Exclusion criteria include major systemic diseases (e.g., heart failure, liver cirrhosis, end-stage renal disease, scleroderma, or diabetes mellitus), history of vasovagal syncope, acute inflammation, nasal or esophageal stenosis/obstruction, upper gastrointestinal symptoms within the past 3 months, use of medications affecting gastrointestinal motility, recent anticoagulant or antiplatelet use within 1 week before enrollment, or bleeding tendency. After informed consent is obtained, participants will fast for 4-8 hours before testing. Assessments will include a rapid swallowing test, anthropometric measurements and InBody analysis, limb ultrasound and muscle strength evaluation using the MicroFET2™ wireless handheld dynamometer and handgrip dynamometer, ultrasonographic assessment of hyoid bone movement and swallowing-related muscles (e.g., masseter muscle), HRIM and VFSS examinations, and blood sampling (5 cc) for biochemical analysis including LDL, HDL, cholesterol, white blood cell count, and hemoglobin.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 18 years or older without subjective swallowing difficulty.

Exclusion criteria

  • (1) Major systemic diseases, including heart failure, liver cirrhosis, end-stage renal disease, scleroderma, or diabetes mellitus; (2) History of vasovagal syncope, acute inflammation, or nasal or esophageal stenosis/obstruction; (3) Presence of upper gastrointestinal symptoms within the past 3 months, including dysphagia, chest pain, heartburn, reflux, or globus sensation; (4) Current use of medications that may affect gastrointestinal motility; (5) Use of anticoagulant or antiplatelet agents within 1 week prior to enrollment; or (6) History of bleeding tendency.

Treatment and study plan

Primary outcomes

  1. hypopharyngeal mean peak pressure

    Time frame: 15 min

    pharyngeal contraction

Study contacts

Contact information is provided by the study sponsor or research team.

Chi-Jun Lai

CONTACT

[email protected]

0972652086

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

Normative Swallowing Physiological Metrics of Pharyngeal High-Resolution Impedance Manometry and Videofluoroscopic Swallowing Study in Chinese Adults

Important dates

Study start
2026
Primary completion
2031
Study completion
2032
First posted
May 19, 2026
Registry last updated
May 19, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.