AzTrials
AzTrials

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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

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.

Reza Shaker, MD contact

4149556840

rshaker@mcw.edu

Mark Kern contact

4148053826

mkern@mcw.edu

United States1 site, 1 recruiting
  • Medical College of Wisconsin

    Milwaukee, Wisconsin, 53086

    Reza Shaker, MD, 4149556840, rshaker@mcw.edu

    Mark Kern, 4148053826, mkern@mcw.edu

    Recruiting

Other trials in United States

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.

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 groups in NCT05708885
Study groupRoleWhat they receive
Striated esophagus deglutitive motor function healthy adultsActive comparatorTesting 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 motilityActive comparatorTesting 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 manometryActive comparatorTesting 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.

  1. 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

  2. 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

  3. hypopharyngeal intra-bolus

    pressure within the swallowed bolus as it passes through the hypopharynx

    Measured: Before exerciser regimen, during deglutitive restriction of the larynx

  4. hypopharyngeal intra-bolus

    pressure within the swallowed bolus as it passes through the hypopharynx

    Measured: After exerciser regimen, during deglutitive restriction of the larynx

  5. upper esophageal sphincter (UES) nadir pressure

    minimum pressure during deglutitive UES relaxation

    Measured: Before six weeks exerciser regimen, during deglutitive restriction of the larynx

  6. upper esophageal sphincter (UES) nadir pressure

    minimum pressure during deglutitive UES relaxation

    Measured: After six weeks exerciser regimen, during deglutitive restriction of the larynx

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  12. 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.

  1. First posted1 Feb 2023
  2. Study start13 Sep 2022
  3. Primary completionApr 2027 (estimated)
  4. Study completionApr 2027 (estimated)

Resources

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)
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

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.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in