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Striated Esophageal Motor Function Modulation in Health and Disease

Primary Purpose

Dysphagia, Esophageal

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
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
Sponsored by
Medical College of Wisconsin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Dysphagia, Esophageal

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Healthy subjects aged 18 to 90 years. Patents with dysphagia but normal high resolution esophageal manometric findings defined by the Chicago classification. Exclusion Criteria: 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. 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.

Sites / Locations

  • Medical College of WisconsinRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

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

Arm Description

Testing of manometric, impedance and biomechanical measurements during swallowing in healthy volunteer adult subjects.

Testing of manometric, impedance and biomechanical measurements during swallowing in adult patients with ineffective esophageal motility.

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.

Outcomes

Primary Outcome Measures

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)
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)
hypopharyngeal intra-bolus
pressure within the swallowed bolus as it passes through the hypopharynx
hypopharyngeal intra-bolus
pressure within the swallowed bolus as it passes through the hypopharynx
upper esophageal sphincter (UES) nadir pressure
minimum pressure during deglutitive UES relaxation
upper esophageal sphincter (UES) nadir pressure
minimum pressure during deglutitive UES relaxation
pharyngeal contractile integral
Time-space integral of the pharynx during swallows as measured from the manometric display
pharyngeal contractile integral
Time-space integral of the pharynx during swallows as measured from the manometric display
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
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
UES anterior-posterior maximum diameter during swallows
maximum deglutitive diameter in the anterior-posterior direction of the UES measured from fluoroscopic images
UES anterior-posterior maximum diameter during swallows
maximum deglutitive diameter in the anterior-posterior direction of the UES measured from fluoroscopic images

Secondary Outcome Measures

Full Information

First Posted
January 13, 2023
Last Updated
February 8, 2023
Sponsor
Medical College of Wisconsin
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1. Study Identification

Unique Protocol Identification Number
NCT05708885
Brief Title
Striated Esophageal Motor Function Modulation in Health and Disease
Official Title
Characterization of the Striated Esophagus (St.Eso) Deglutitive Motor Function and Its Modulation by Pharyngeal Phase Swallow Biomechanics
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 13, 2022 (Actual)
Primary Completion Date
April 2026 (Anticipated)
Study Completion Date
April 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical College of Wisconsin

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dysphagia, Esophageal

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
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)
Allocation
Non-Randomized
Enrollment
557 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Striated esophagus deglutitive motor function healthy adults
Arm Type
Active Comparator
Arm Description
Testing of manometric, impedance and biomechanical measurements during swallowing in healthy volunteer adult subjects.
Arm Title
Striated esophagus deglutitive motor function in patients with ineffective esophageal motility
Arm Type
Active Comparator
Arm Description
Testing of manometric, impedance and biomechanical measurements during swallowing in adult patients with ineffective esophageal motility.
Arm Title
Striated esophagus deglutitive motor function patients with symptoms but normal esophageal manometry
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Device
Intervention Name(s)
Concurrent manometry/impedance and fluoroscopy with and without laryngeal restriction
Intervention Description
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.
Intervention Type
Device
Intervention Name(s)
Concurrent manometry/impedance and fluoroscopy before and after six weeks of using swallow muscle exercising device
Intervention Description
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.
Primary Outcome Measure Information:
Title
peak deglutitive pharyngeal peristaltic wave pressure
Description
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)
Time Frame
Before six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
peak deglutitive pharyngeal peristaltic wave pressure
Description
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)
Time Frame
After six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
hypopharyngeal intra-bolus
Description
pressure within the swallowed bolus as it passes through the hypopharynx
Time Frame
Before exerciser regimen, during deglutitive restriction of the larynx
Title
hypopharyngeal intra-bolus
Description
pressure within the swallowed bolus as it passes through the hypopharynx
Time Frame
After exerciser regimen, during deglutitive restriction of the larynx
Title
upper esophageal sphincter (UES) nadir pressure
Description
minimum pressure during deglutitive UES relaxation
Time Frame
Before six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
upper esophageal sphincter (UES) nadir pressure
Description
minimum pressure during deglutitive UES relaxation
Time Frame
After six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
pharyngeal contractile integral
Description
Time-space integral of the pharynx during swallows as measured from the manometric display
Time Frame
Before six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
pharyngeal contractile integral
Description
Time-space integral of the pharynx during swallows as measured from the manometric display
Time Frame
After six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
maximum excursion of the hyo-laryngeal complex
Description
maximum deglutitive excursion of the hyoid and larynx from the pre-swallow resting position as measured from fluoroscopic images
Time Frame
Before six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
maximum excursion of the hyo-laryngeal complex
Description
maximum deglutitive excursion of the hyoid and larynx from the pre-swallow resting position as measured from fluoroscopic images
Time Frame
After six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
UES anterior-posterior maximum diameter during swallows
Description
maximum deglutitive diameter in the anterior-posterior direction of the UES measured from fluoroscopic images
Time Frame
Before six weeks exerciser regimen, during deglutitive restriction of the larynx
Title
UES anterior-posterior maximum diameter during swallows
Description
maximum deglutitive diameter in the anterior-posterior direction of the UES measured from fluoroscopic images
Time Frame
After six weeks exerciser regimen, during deglutitive restriction of the larynx

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy subjects aged 18 to 90 years. Patents with dysphagia but normal high resolution esophageal manometric findings defined by the Chicago classification. Exclusion Criteria: 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. 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Reza Shaker, MD
Phone
4149556840
Email
rshaker@mcw.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Mark Kern
Phone
4148053826
Email
mkern@mcw.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Reza Shaker
Organizational Affiliation
Medical College of Wisconsin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical College of Wisconsin
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53086
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Reza Shaker, MD
Phone
414-955-6840
Email
rshaker@mcw.edu
First Name & Middle Initial & Last Name & Degree
Mark Kern
Phone
4148053826
Email
mkern@mcw.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Striated Esophageal Motor Function Modulation in Health and Disease

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