Dysphagia, EsophagealNCT05708885
Striated Esophageal Motor Function Modulation in Health and Disease
A study testing Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction and Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising device in people with Dysphagia, Esophageal, run by Medical College of Wisconsin at 1 site in United States.
Trial summary
The investigators hypothesize that striated esophagus deglutitive motor function is modulated by pharyngeal phase swallowing biomechanics. Read more about this study
- Who is it for?
- Ages 18 to 90 yearsHealthy volunteers can take part
- Conditions the study is for
- Dysphagia, Esophageal
- What is being tested?
- Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction and Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising device
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 557 participants
- Where
- 1 siteUnited States
- Study dates
- 13 Sep 2022to Apr 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 90 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Healthy subjects aged 18 to 90 years.
- Patents with dysphagia but normal high resolution esophageal manometric findings defined by the Chicago classification.
Who cannot join
- Anyone less than 18 years old.
- Patients with recent head and neck cancer (<1 month post-surgery or <3 months post-chemo radiation.
- Patients suffering from muscle diseases like muscular dystrophies, myopathies.
- Patients with neuro-muscular junction disorders myasthenia gravis, Eaton-Lambert disorders.
- Patients having history of allergy to lidocaine or barium.
- Patients who are pregnant or lactating.
Show all 9Show fewer
- Patients who are medically unstable.
- Patients who are unable to apply the exerciser independently or with the help of a caregiver.
- Patients who lack cognition.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site, 1 recruiting
- Recruiting
Medical College of Wisconsin
Milwaukee, Wisconsin, 53086
Reza Shaker, MD, 4149556840, rshaker@mcw.edu
Mark Kern, 4148053826, mkern@mcw.edu
About this study
Official title: Characterization of the Striated Esophagus (St.Eso) Deglutitive Motor Function and Its Modulation by Pharyngeal Phase Swallow Biomechanics
The investigators hypothesize that striated esophagus deglutitive motor function is modulated by pharyngeal phase swallowing biomechanics.
Read the detailed description
To achieve the specific aim, the investigators will use state-of the-art available techniques and recording modalities alone or in combination/concurrently, as well as a novel device with proven ability to non-invasively manipulate the pharyngeal biomechanics both in a positive as well as negative way. This device and technique have been described earlier in the innovation section.
High Resolution Manometry (HRM)/Impedance recording: Pharyngeal and proximal esophageal pressure phenomena will be recorded and analyzed using a high-resolution manometric catheter (36 sensors 1 cm spacing), positioned trans-nasally to traverse the pharynx, UES, and proximal esophagus passing the transition zone) and computerized recording and analysis system. Also, manometric data will be imported to a supplementary programming environment when computational tools provided in the conventional software do not meet our analytical needs. Also configured on the high-resolution manometric probe are 18 impedance sites spaced every 2 cm to monitor bolus position. Similar to the manometric data, impedance data is also displayed by the previously described recording and analysis systems.
Concurrent high-resolution impedance manometry and digital video-fluoroscopic recording: To obtain objective quantifiable measures of peristalsis, swallow biomechanics and bolus kinematics, the investigators use high resolution impedance manometry concurrent with 30 frame/sec digital videofluoroscopy. Since our catheter also has impedance recording it will provide opportunity for additional analysis in concert with fluoroscopic recordings.
Digital video-fluoroscopy: The investigators will use digital video fluoroscopy at 30 frame/s in the sagittal or frontal view to record and subsequently analyze the deglutitive laryngeal and hyoid excursions as well as UES opening and closure data and bolus trajectory and kinematics. Video-fluoroscopic recordings will be obtained at 90 kiloelectron volt, using a 9-in. image intensifier and appropriate collimation. Based on our preliminary studies, the investigators will record 5-ml and 10-ml liquid barium swallows. Fluoroscopic sagittal images will be targeted to clearly visualize the entire pharynx, larynx, hyoid bone, upper esophageal sphincter (UES) and the proximal esophagus. A pregnancy testing will be completed prior to fluoroscopy exposure.
Technique for reducing laryngeal and striated esophagus (St.Eso) excursion: the investigators will use the swallowing resistance exercise device (sRED) to experimentally reduce the laryngeal and St.Eso excursion and UES opening.
Technique for increasing the laryngeal and St.Eso excursion. The investigators will deploy the strength training exercise protocol using the s-RED device published previously which has shown to result in significant increase in laryngeal excursion and UES opening.
In healthy and patient volunteers, the investigators will determine and characterize the non-peristaltic and peristaltic components of the St.Eso motor functions and their relationship with pharyngeal phase biomechanics.
Study subjects: The investigators will study a total of 120 healthy volunteers from six consecutive decades 18-30, 31-40,41-50,51-60 and older than 70 years (20 /group, 10F) as well as 20 patients with dysphagia symptom but normal manometry (Sympt N) and 20 patients with Ineffective Esophageal Motility (IEM) all according to Chicago Classification. The inclusion of consecutive decades in addition to deciphering the age effect will provide the healthy age and sex randomly matched controls for the two patients groups.
Study technique: Concurrent manometry/Impedance and digital video-fluoroscopy in upright and supine positions.
Study boluses: 5- and 10-mL liquid and 5mm barium pellet each x5 (30s. interval).
In healthy and patient volunteers, the investigators will determine and characterize the effect of experimentally enhancing and reducing pharyngeal biomechanics on St.Eso. motor functions,
Study subjects: The investigators will study 40 elderlies over the age of 70 years, 40 patients with dysphagia symptom but normal HRM manometry and 40 IEM patients. Studies will be done in three conditions: Baseline, experimentally decreased and increased laryngeal excursion. Study technique, bolus size and analysis will be the same for all three stages. After completion of baseline studies, in the same session the investigators will repeat the study with application of the S-RED and repeat the swallows with s-RED in place at zero pressure and at 40 mmHg pressure applied randomly (using an a-priori selected random table).
After completion of this stage subjects will be randomly assigned 1:1 to do the s-RED assisted or a sham (tongue protrusion) exercise three times a day for six weeks the investigators have phone follow up methods to ensure compliance. Studies will be repeated in each subject during the week following the completion of six weeks exercises. Subjects will be instructed to continue their exercise until they are re-studied. The post exercise study will be the same as the baseline study and without use of the s-RED device. Comparisons will be made between the data from baseline studies and both real and sham exercise results as well as between real and sham exercises.
Study technique: Concurrent HRM/Impedance and digital video-fluoroscopy in upright and supine positions.
Study boluses: 5- and 10-mL liquid barium each x5 (30s. interval).
Technique for reducing laryngeal and St.Eso excursion: the investigators will use the sRED device described below section to experimentally reduce the laryngeal and St.Eso excursion and UES opening.
Device for reducing laryngeal/St.Eso excursion
To quantitively reduce the laryngeal movement and St.Eso excursion the investigators will use a device constructed in our laboratory which can induce an adjustable resistance to anterior and superior excursion of the larynx. This handmade device that is worn around the neck consists of two parts described previously, a band and a concave plastic disk which serves as a support structure for an inflatable polyethylene bag which is connected to a hand pump and pressure gauge. When worn around the neck the inflatable bag rests in position on the thyroid cartilage with a portion of it hung over above the cartilage creating resistance to its superior excursion when fixed by closure of a velcro straps. A known external force may be applied to the thyroid by partially inflating the bag to a specific pressure reading on the gauge. The soft and compliant bag conforms to the surface of the skin cradling the irregular geometry of the larynx while applying a resistive force to anterior and superior distraction of the hyolaryngeal complex during swallowing. Earlier studies have shown a direct relationship between the anterosuperior excursion of the thyroid cartilage, and the pressure applied by this device.
Technique for increasing the laryngeal and St.Eso excursion. The investigators will deploy the strength training exercise protocol using the s-RED device published previously which has shown to result in significant increase in laryngeal excursion and UES opening.
Technique for increasing anterosuperior excursion of the larynx and St.Eso: Earlier studies in our lab and others have shown that laryngeal and hyoid deglutitive excursion is significantly reduced in the elderly compared to young. Other studies using strength training exercises including those using the above-mentioned device have shown significant improvement in this reduction. The information provided by these studies suggest that elderly individuals are a suitable model for testing the effect of increase in laryngeal/St.Eso excursion on the motor function of the St.Eso. Therefore, the investigators will study elderly as a natural physiologic model of reduced laryngeal/St.Eso excursion and use the above-mentioned wearable device and exercise regimen described previously for studying the effect of increase in anterosuperior excursion of the larynx/St.Eso on St.Eso peristaltic function. These experiments may also provide mechanistic information on reports suggesting an association between esophageal dysmotility and oropharyngeal dysphagia and positive effect of swallowing maneuvers on esophageal peristalsis.
In healthy and patient volunteers, the investigators will determine and characterize the St.Eso peristalsis parameters and its modulation by bolus type, volume, body positions and age.
Study subjects: The investigators will study a total of 120 healthy volunteers from six consecutive decades 18-30, 31-40,41-50,51-60 and older than 70 years (20 /group, 10F) as well as 20 patients with Sympt N and 20 patients IEM. Since satiated muscles of St.Eso are subject to age effects, these experiments will also provide normalcy age specific data for future studies by others and will be shared with the community of investigators along with data from the entire project. Data obtained from these studies will fill a significant gap in our understanding of the St.Eso peristalsis specially across the age spectrum as well as in motility disorders.
Study technique: Concurrent HRM/Impedance recording in upright and supine positions.
Study boluses: 5- and 10-mL boluses of water, and 5 mL Vicious bolus each x10 (30s. interval). In addition, in each subject the investigators will perform multiple rapid swallow test in upright and supine positions to determine the functional reserve of the St.Eso across the age.
- Conditions
- Dysphagia, Esophageal
- Being tested
- Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction, Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising device
- Medical subject headings
- Deglutition Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Concurrent manometry/impedance and fluoroscopy with and without laryngeal restrictionDevice
To reduce the laryngeal movement and St.Eso excursion we will use a device constructed in our laboratory which can induce an adjustable resistance to excursion of the larynx. This handmade device that is worn around the neck consists of a band and a concave plastic disk which serves as a support structure for an inflatable polyethylene bag which is connected to a hand pump and pressure gauge. When worn around the neck the inflatable bag rests in position on the thyroid cartilage with a portion of it hung over above the cartilage creating resistance to its superior excursion when fixed by closure straps. A known external force may be applied to the thyroid by partially inflating the bag to a specific pressure reading on the gauge. The soft and compliant bag conforms to the larynx while applying a resistive force to anterior and superior distraction of the hyolaryngeal complex during swallowing.
Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising deviceDevice
Use the previously mentioned wearable device (sRED) and exercise regimen described previously for studying the effect of increase in anterosuperior excursion of the larynx/St.Eso on St.Eso peristaltic function.
| Study group | Role | What they receive |
|---|---|---|
| Striated esophagus deglutitive motor function healthy adults | Active comparator | Testing of manometric, impedance and biomechanical measurements during swallowing in healthy volunteer adult subjects. Receives: Device: Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction; Device: Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising device |
| Striated esophagus deglutitive motor function in patients with ineffective esophageal motility | Active comparator | Testing of manometric, impedance and biomechanical measurements during swallowing in adult patients with ineffective esophageal motility. Receives: Device: Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction; Device: Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising device |
| Striated esophagus deglutitive motor function patients with symptoms but normal esophageal manometry | Active comparator | Testing of manometric, impedance and biomechanical measurements during swallowing in adult patients with symptoms of dysphagia but "normal" esophageal manometry by the Chicago Classification criteria. Receives: Device: Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction; Device: Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising device |
What is being measured
The primary outcome is the main question the study is designed to answer.
peak deglutitive pharyngeal peristaltic wave pressure
Peak deglutitive pharyngeal peristaltic wave pressure will be measured at positions 2-8cm above the upper margin of the manometrically determined upper esophageal sphincter high-pressure zone (UESHPZ)
Measured: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
peak deglutitive pharyngeal peristaltic wave pressure
Peak deglutitive pharyngeal peristaltic wave pressure will be measured at positions 2-8cm above the upper margin of the manometrically determined upper esophageal sphincter high-pressure zone (UESHPZ)
Measured: After six weeks exerciser regimen, during deglutitive restriction of the larynx
hypopharyngeal intra-bolus
pressure within the swallowed bolus as it passes through the hypopharynx
Measured: Before exerciser regimen, during deglutitive restriction of the larynx
hypopharyngeal intra-bolus
pressure within the swallowed bolus as it passes through the hypopharynx
Measured: After exerciser regimen, during deglutitive restriction of the larynx
upper esophageal sphincter (UES) nadir pressure
minimum pressure during deglutitive UES relaxation
Measured: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
upper esophageal sphincter (UES) nadir pressure
minimum pressure during deglutitive UES relaxation
Measured: After six weeks exerciser regimen, during deglutitive restriction of the larynx
pharyngeal contractile integral
Time-space integral of the pharynx during swallows as measured from the manometric display
Measured: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
pharyngeal contractile integral
Time-space integral of the pharynx during swallows as measured from the manometric display
Measured: After six weeks exerciser regimen, during deglutitive restriction of the larynx
maximum excursion of the hyo-laryngeal complex
maximum deglutitive excursion of the hyoid and larynx from the pre-swallow resting position as measured from fluoroscopic images
Measured: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
maximum excursion of the hyo-laryngeal complex
maximum deglutitive excursion of the hyoid and larynx from the pre-swallow resting position as measured from fluoroscopic images
Measured: After six weeks exerciser regimen, during deglutitive restriction of the larynx
UES anterior-posterior maximum diameter during swallows
maximum deglutitive diameter in the anterior-posterior direction of the UES measured from fluoroscopic images
Measured: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
UES anterior-posterior maximum diameter during swallows
maximum deglutitive diameter in the anterior-posterior direction of the UES measured from fluoroscopic images
Measured: After six weeks exerciser regimen, during deglutitive restriction of the larynx
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Feb 2023
- Study start13 Sep 2022
- Primary completionApr 2027 (estimated)
- Study completionApr 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Dysphagia, EsophagealStudies of the same condition, open and under way.
- More trials run by Medical College of WisconsinThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Model description
- Testing the hypothesis that striated esophagus deglutitive motor function is modulated by pharyngeal phase swallowing biomechanics in health and disease.
- Masking
- None (open label)
- Enrolment
- 557 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Medical College of Wisconsin
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Reza Shaker, MD, Medical College of Wisconsin
- Investigators
- Reza Shaker, Principal investigator, Medical College of Wisconsin
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05708885
- Sponsor's protocol ID
- PRO00042719
- Status last verified
- Apr 2026
- First submitted
- 13 Jan 2023
- Last updated
- 5 May 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Characterization of the Striated Esophagus (St.Eso) Deglutitive Motor Function and Its Modulation by Pharyngeal Phase Swallow Biomechanics
- ClinicalTrials.gov ID
- NCT05708885
- Acronym / sponsor ID
- PRO00042719
- Conditions
- Dysphagia, Esophageal
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 557 participants (estimated)
- Lead sponsor
- Medical College of WisconsinUniversity, hospital or other
- Study start
- 13 Sep 2022 (actual)
- Primary completion
- Apr 2027 (estimated)
- Study completion
- Apr 2027 (estimated)
- First posted
- 1 Feb 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The investigators hypothesize that striated esophagus deglutitive motor function is modulated by pharyngeal phase swallowing biomechanics.
Detailed description
To achieve the specific aim, the investigators will use state-of the-art available techniques and recording modalities alone or in combination/concurrently, as well as a novel device with proven ability to non-invasively manipulate the pharyngeal biomechanics both in a positive as well as negative way. This device and technique have been described earlier in the innovation section.
High Resolution Manometry (HRM)/Impedance recording: Pharyngeal and proximal esophageal pressure phenomena will be recorded and analyzed using a high-resolution manometric catheter (36 sensors 1 cm spacing), positioned trans-nasally to traverse the pharynx, UES, and proximal esophagus passing the transition zone) and computerized recording and analysis system. Also, manometric data will be imported to a supplementary programming environment when computational tools provided in the conventional software do not meet our analytical needs. Also configured on the high-resolution manometric probe are 18 impedance sites spaced every 2 cm to monitor bolus position. Similar to the manometric data, impedance data is also displayed by the previously described recording and analysis systems.
Concurrent high-resolution impedance manometry and digital video-fluoroscopic recording: To obtain objective quantifiable measures of peristalsis, swallow biomechanics and bolus kinematics, the investigators use high resolution impedance manometry concurrent with 30 frame/sec digital videofluoroscopy. Since our catheter also has impedance recording it will provide opportunity for additional analysis in concert with fluoroscopic recordings.
Digital video-fluoroscopy: The investigators will use digital video fluoroscopy at 30 frame/s in the sagittal or frontal view to record and subsequently analyze the deglutitive laryngeal and hyoid excursions as well as UES opening and closure data and bolus trajectory and kinematics. Video-fluoroscopic recordings will be obtained at 90 kiloelectron volt, using a 9-in. image intensifier and appropriate collimation. Based on our preliminary studies, the investigators will record 5-ml and 10-ml liquid barium swallows. Fluoroscopic sagittal images will be targeted to clearly visualize the entire pharynx, larynx, hyoid bone, upper esophageal sphincter (UES) and the proximal esophagus. A pregnancy testing will be completed prior to fluoroscopy exposure.
Technique for reducing laryngeal and striated esophagus (St.Eso) excursion: the investigators will use the swallowing resistance exercise device (sRED) to experimentally reduce the laryngeal and St.Eso excursion and UES opening.
Technique for increasing the laryngeal and St.Eso excursion. The investigators will deploy the strength training exercise protocol using the s-RED device published previously which has shown to result in significant increase in laryngeal excursion and UES opening.
In healthy and patient volunteers, the investigators will determine and characterize the non-peristaltic and peristaltic components of the St.Eso motor functions and their relationship with pharyngeal phase biomechanics.
Study subjects: The investigators will study a total of 120 healthy volunteers from six consecutive decades 18-30, 31-40,41-50,51-60 and older than 70 years (20 /group, 10F) as well as 20 patients with dysphagia symptom but normal manometry (Sympt N) and 20 patients with Ineffective Esophageal Motility (IEM) all according to Chicago Classification. The inclusion of consecutive decades in addition to deciphering the age effect will provide the healthy age and sex randomly matched controls for the two patients groups.
Study technique: Concurrent manometry/Impedance and digital video-fluoroscopy in upright and supine positions.
Study boluses: 5- and 10-mL liquid and 5mm barium pellet each x5 (30s. interval).
In healthy and patient volunteers, the investigators will determine and characterize the effect of experimentally enhancing and reducing pharyngeal biomechanics on St.Eso. motor functions,
Study subjects: The investigators will study 40 elderlies over the age of 70 years, 40 patients with dysphagia symptom but normal HRM manometry and 40 IEM patients. Studies will be done in three conditions: Baseline, experimentally decreased and increased laryngeal excursion. Study technique, bolus size and analysis will be the same for all three stages. After completion of baseline studies, in the same session the investigators will repeat the study with application of the S-RED and repeat the swallows with s-RED in place at zero pressure and at 40 mmHg pressure applied randomly (using an a-priori selected random table).
After completion of this stage subjects will be randomly assigned 1:1 to do the s-RED assisted or a sham (tongue protrusion) exercise three times a day for six weeks the investigators have phone follow up methods to ensure compliance. Studies will be repeated in each subject during the week following the completion of six weeks exercises. Subjects will be instructed to continue their exercise until they are re-studied. The post exercise study will be the same as the baseline study and without use of the s-RED device. Comparisons will be made between the data from baseline studies and both real and sham exercise results as well as between real and sham exercises.
Study technique: Concurrent HRM/Impedance and digital video-fluoroscopy in upright and supine positions.
Study boluses: 5- and 10-mL liquid barium each x5 (30s. interval).
Technique for reducing laryngeal and St.Eso excursion: the investigators will use the sRED device described below section to experimentally reduce the laryngeal and St.Eso excursion and UES opening.
Device for reducing laryngeal/St.Eso excursion
To quantitively reduce the laryngeal movement and St.Eso excursion the investigators will use a device constructed in our laboratory which can induce an adjustable resistance to anterior and superior excursion of the larynx. This handmade device that is worn around the neck consists of two parts described previously, a band and a concave plastic disk which serves as a support structure for an inflatable polyethylene bag which is connected to a hand pump and pressure gauge. When worn around the neck the inflatable bag rests in position on the thyroid cartilage with a portion of it hung over above the cartilage creating resistance to its superior excursion when fixed by closure of a velcro straps. A known external force may be applied to the thyroid by partially inflating the bag to a specific pressure reading on the gauge. The soft and compliant bag conforms to the surface of the skin cradling the irregular geometry of the larynx while applying a resistive force to anterior and superior distraction of the hyolaryngeal complex during swallowing. Earlier studies have shown a direct relationship between the anterosuperior excursion of the thyroid cartilage, and the pressure applied by this device.
Technique for increasing the laryngeal and St.Eso excursion. The investigators will deploy the strength training exercise protocol using the s-RED device published previously which has shown to result in significant increase in laryngeal excursion and UES opening.
Technique for increasing anterosuperior excursion of the larynx and St.Eso: Earlier studies in our lab and others have shown that laryngeal and hyoid deglutitive excursion is significantly reduced in the elderly compared to young. Other studies using strength training exercises including those using the above-mentioned device have shown significant improvement in this reduction. The information provided by these studies suggest that elderly individuals are a suitable model for testing the effect of increase in laryngeal/St.Eso excursion on the motor function of the St.Eso. Therefore, the investigators will study elderly as a natural physiologic model of reduced laryngeal/St.Eso excursion and use the above-mentioned wearable device and exercise regimen described previously for studying the effect of increase in anterosuperior excursion of the larynx/St.Eso on St.Eso peristaltic function. These experiments may also provide mechanistic information on reports suggesting an association between esophageal dysmotility and oropharyngeal dysphagia and positive effect of swallowing maneuvers on esophageal peristalsis.
In healthy and patient volunteers, the investigators will determine and characterize the St.Eso peristalsis parameters and its modulation by bolus type, volume, body positions and age.
Study subjects: The investigators will study a total of 120 healthy volunteers from six consecutive decades 18-30, 31-40,41-50,51-60 and older than 70 years (20 /group, 10F) as well as 20 patients with Sympt N and 20 patients IEM. Since satiated muscles of St.Eso are subject to age effects, these experiments will also provide normalcy age specific data for future studies by others and will be shared with the community of investigators along with data from the entire project. Data obtained from these studies will fill a significant gap in our understanding of the St.Eso peristalsis specially across the age spectrum as well as in motility disorders.
Study technique: Concurrent HRM/Impedance recording in upright and supine positions.
Study boluses: 5- and 10-mL boluses of water, and 5 mL Vicious bolus each x10 (30s. interval). In addition, in each subject the investigators will perform multiple rapid swallow test in upright and supine positions to determine the functional reserve of the St.Eso across the age.
Study design
- Primary purpose
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- Testing the hypothesis that striated esophagus deglutitive motor function is modulated by pharyngeal phase swallowing biomechanics in health and disease.
| Arm | Type | Receives |
|---|---|---|
| Striated esophagus deglutitive motor function healthy adults | Active comparator | Device: Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction, Device: Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising deviceTesting of manometric, impedance and biomechanical measurements during swallowing in healthy volunteer adult subjects. |
| Striated esophagus deglutitive motor function in patients with ineffective esophageal motility | Active comparator | Device: Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction, Device: Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising deviceTesting of manometric, impedance and biomechanical measurements during swallowing in adult patients with ineffective esophageal motility. |
| Striated esophagus deglutitive motor function patients with symptoms but normal esophageal manometry | Active comparator | Device: Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction, Device: Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising deviceTesting of manometric, impedance and biomechanical measurements during swallowing in adult patients with symptoms of dysphagia but "normal" esophageal manometry by the Chicago Classification criteria. |
Who may qualify
- Ages
- 18 to 90 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Healthy subjects aged 18 to 90 years.
- Patents with dysphagia but normal high resolution esophageal manometric findings defined by the Chicago classification.
Key exclusion criteria (9 listed)
- Anyone less than 18 years old.
- Patients with recent head and neck cancer (<1 month post-surgery or <3 months post-chemo radiation.
- Patients suffering from muscle diseases like muscular dystrophies, myopathies.
- Patients with neuro-muscular junction disorders myasthenia gravis, Eaton-Lambert disorders.
- Patients having history of allergy to lidocaine or barium.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Concurrent manometry/impedance and fluoroscopy with and without laryngeal restrictionTo reduce the laryngeal movement and St.Eso excursion we will use a device constructed in our laboratory which can induce an adjustable resistance to excursion of the larynx. This handmade device that is worn around the neck consists of a band and a concave plastic disk which serves as a support structure for an inflatable polyethylene bag which is connected to a hand pump and pressure gauge. When worn around the neck the inflatable bag rests in position on the thyroid cartilage with a portion of it hung over above the cartilage creating resistance to its superior excursion when fixed by closure straps. A known external force may be applied to the thyroid by partially inflating the bag to a specific pressure reading on the gauge. The soft and compliant bag conforms to the larynx while applying a resistive force to anterior and superior distraction of the hyolaryngeal complex during swallowing. | Device | Striated esophagus deglutitive motor function healthy adults, Striated esophagus deglutitive motor function in patients with ineffective esophageal motility, Striated esophagus deglutitive motor function patients with symptoms but normal esophageal manometry |
| Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising deviceUse the previously mentioned wearable device (sRED) and exercise regimen described previously for studying the effect of increase in anterosuperior excursion of the larynx/St.Eso on St.Eso peristaltic function. | Device | Striated esophagus deglutitive motor function healthy adults, Striated esophagus deglutitive motor function in patients with ineffective esophageal motility, Striated esophagus deglutitive motor function patients with symptoms but normal esophageal manometry |
Primary outcome
peak deglutitive pharyngeal peristaltic wave pressure
Time frame: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
Peak deglutitive pharyngeal peristaltic wave pressure will be measured at positions 2-8cm above the upper margin of the manometrically determined upper esophageal sphincter high-pressure zone (UESHPZ)
peak deglutitive pharyngeal peristaltic wave pressure
Time frame: After six weeks exerciser regimen, during deglutitive restriction of the larynx
Peak deglutitive pharyngeal peristaltic wave pressure will be measured at positions 2-8cm above the upper margin of the manometrically determined upper esophageal sphincter high-pressure zone (UESHPZ)
hypopharyngeal intra-bolus
Time frame: Before exerciser regimen, during deglutitive restriction of the larynx
pressure within the swallowed bolus as it passes through the hypopharynx
hypopharyngeal intra-bolus
Time frame: After exerciser regimen, during deglutitive restriction of the larynx
pressure within the swallowed bolus as it passes through the hypopharynx
upper esophageal sphincter (UES) nadir pressure
Time frame: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
minimum pressure during deglutitive UES relaxation
upper esophageal sphincter (UES) nadir pressure
Time frame: After six weeks exerciser regimen, during deglutitive restriction of the larynx
minimum pressure during deglutitive UES relaxation
pharyngeal contractile integral
Time frame: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
Time-space integral of the pharynx during swallows as measured from the manometric display
pharyngeal contractile integral
Time frame: After six weeks exerciser regimen, during deglutitive restriction of the larynx
Time-space integral of the pharynx during swallows as measured from the manometric display
maximum excursion of the hyo-laryngeal complex
Time frame: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
maximum deglutitive excursion of the hyoid and larynx from the pre-swallow resting position as measured from fluoroscopic images
maximum excursion of the hyo-laryngeal complex
Time frame: After six weeks exerciser regimen, during deglutitive restriction of the larynx
maximum deglutitive excursion of the hyoid and larynx from the pre-swallow resting position as measured from fluoroscopic images
UES anterior-posterior maximum diameter during swallows
Time frame: Before six weeks exerciser regimen, during deglutitive restriction of the larynx
maximum deglutitive diameter in the anterior-posterior direction of the UES measured from fluoroscopic images
UES anterior-posterior maximum diameter during swallows
Time frame: After six weeks exerciser regimen, during deglutitive restriction of the larynx
maximum deglutitive diameter in the anterior-posterior direction of the UES measured from fluoroscopic images
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 May 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Reza Shaker principal investigator
Medical College of Wisconsin
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction and Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising device in people with Dysphagia, Esophageal, run by Medical College of Wisconsin at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 5 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Reza Shaker, MD (4149556840, rshaker@mcw.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
peak deglutitive pharyngeal peristaltic wave pressure (time frame: Before six weeks exerciser regimen, during deglutitive restriction of the larynx). The study lists 12 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 May 2026.