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Mechanisms and Management of Infant Dysphagia

Primary Purpose

Dysphagia, Airway Aspiration, Airway Penetration

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Combined testing (diagnostic VFSS + research HRM) + Parent Preferred Therapy
Sponsored by
Sudarshan Jadcherla
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Dysphagia focused on measuring Infant, Feeding difficulties, Dysphagia

Eligibility Criteria

38 Weeks - 60 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants with feeding-related aero-digestive symptoms
  • ≤60 weeks PMA (both pre-term and full term)
  • History of orally feeding ≥ 25% of least 50% of prescribed feeding volume
  • Room air or supplemental oxygen of ≤1liter/minute (LPM)

Exclusion Criteria:

  • Direct breast feeding exclusively
  • Known genetic, metabolic or syndromic disease
  • Neurological diseases such as Grade 3 or 4 intraventricular hemorrhage (IVH) or intracranial hemorrhage (ICH), moderate to severe perinatal asphyxia or stroke
  • Craniofacial, airway or foregut malformations
  • History of craniofacial, foregut, ears, nose and throat (ENT) or neurosurgery

Sites / Locations

  • The Research Institute at Nationwide Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Study

Control

Arm Description

Eligible subjects (study) will undergo diagnostic VFSS in combination with manometry, either concurrent or sequential. They will have parental choice of preferred feeding therapy.

Eligible subjects who had VFSS alone with provider recommendations from the same single center.

Outcomes

Primary Outcome Measures

Number of Participants With Successful Safe Oral Feeding
The primary endpoint is the feeding success defined as full oral feeding (no tube feeds feeds) without symptoms that require interventions

Secondary Outcome Measures

Weight Growth Velocity in Grams/Day
The investigators will measure and track growth velocity (grams/day) during this time period. This will be completed through chart reviews of weight from subsequent clinic visits and parent interviews.
Hospital Length of Stay From Admission to Discharge in Days
The investigators will track the subjects length of hospitalization which included their initial study procedure.

Full Information

First Posted
October 20, 2015
Last Updated
August 19, 2021
Sponsor
Sudarshan Jadcherla
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Ohio State University, Medical College of Wisconsin
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1. Study Identification

Unique Protocol Identification Number
NCT02583360
Brief Title
Mechanisms and Management of Infant Dysphagia
Official Title
Neonatal Esophagus and Airway Interactions in Health and Disease
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
October 2, 2015 (Actual)
Primary Completion Date
August 30, 2020 (Actual)
Study Completion Date
August 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sudarshan Jadcherla
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Ohio State University, Medical College of Wisconsin

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the investigator's study is to evaluate the causes of feeding difficulty in infants. New treatments can be possible only if the cause is known. In this study, the investigator plans to evaluate the movement of the muscles in an infant's mouth, throat (pharynx) and food pipe (esophagus) that are responsible for moving the food down into the stomach and that help protect an infants airway.
Detailed Description
Infants with chronic feeding difficulties exhibit inadequacy of suck-swallow and breathe coordination, regurgitation or vomiting, gastroesophageal reflux disease, and airway aspiration. Often these infants must rely on feeding tubes, either inserted through the nose or surgically placed, to meet their nutrition and hydration needs until they are able to orally feed safely, effectively, and efficiently. The process of assessment and treatment of swallowing disorders is often stressful for the infants and their providers, including parents. The goal of this study is to combine two commonly used diagnostic techniques (video fluoroscopy swallow studies and esophageal manometry) to more comprehensively evaluate feeding from the mouth to the stomach in infants. The hope is that by doing so treatment strategies can be improved. : Eligible subjects (study) will undergo diagnostic VFSS in combination with manometry, either concurrent or sequential. They will have parental choice of preferred feeding therapy. The data is from single center prospective observational study. The controls are those who had VFSS alone with provider recommendations from the same single center. In addition, we are also embarking on alternate strategies to achieve the original stated aims: 1) Mechanisms of dysphagia is ascertained by studying concurrent recordings of VFSS and manometry. 2) Feeding outcomes of Dysphagic infants are ascertained by evaluating the discharge outcomes and 1-year feeding outcomes among those that had evaluation of dysphagia using VFSS. 3) Dysphagic infants that had sequential VFSS and manometry studies are evaluated to test which method is a better predictor of stated outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dysphagia, Airway Aspiration, Airway Penetration
Keywords
Infant, Feeding difficulties, Dysphagia

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Eligible consented subjects (study) from a single center will undergo standard of care diagnostic VFSS in combination with the research intervention of utilizing manometry procedures to measure pharyngo-esophageal motility to aid with precise diagnosis, either concurrent or sequential. They will then have parental choice of preferred feeding therapy based on combined testing methods rather than therapy being prescribed by the VFSS results. The controls are those who had VFSS alone (standard of care) with treatment based solely on VFSS guided provider recommendations from the same single center.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
109 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study
Arm Type
Active Comparator
Arm Description
Eligible subjects (study) will undergo diagnostic VFSS in combination with manometry, either concurrent or sequential. They will have parental choice of preferred feeding therapy.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Eligible subjects who had VFSS alone with provider recommendations from the same single center.
Intervention Type
Diagnostic Test
Intervention Name(s)
Combined testing (diagnostic VFSS + research HRM) + Parent Preferred Therapy
Intervention Description
Addition of research HRM along with diagnostic VFSS with parental choice of therapy
Primary Outcome Measure Information:
Title
Number of Participants With Successful Safe Oral Feeding
Description
The primary endpoint is the feeding success defined as full oral feeding (no tube feeds feeds) without symptoms that require interventions
Time Frame
Up to 4 weeks after enrollment
Secondary Outcome Measure Information:
Title
Weight Growth Velocity in Grams/Day
Description
The investigators will measure and track growth velocity (grams/day) during this time period. This will be completed through chart reviews of weight from subsequent clinic visits and parent interviews.
Time Frame
4 weeks
Title
Hospital Length of Stay From Admission to Discharge in Days
Description
The investigators will track the subjects length of hospitalization which included their initial study procedure.
Time Frame
from hospital admission until discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
38 Weeks
Maximum Age & Unit of Time
60 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants with feeding-related aero-digestive symptoms ≤60 weeks PMA (both pre-term and full term) History of orally feeding ≥ 25% of least 50% of prescribed feeding volume Room air or supplemental oxygen of ≤1liter/minute (LPM) Exclusion Criteria: Direct breast feeding exclusively Known genetic, metabolic or syndromic disease Neurological diseases such as Grade 3 or 4 intraventricular hemorrhage (IVH) or intracranial hemorrhage (ICH), moderate to severe perinatal asphyxia or stroke Craniofacial, airway or foregut malformations History of craniofacial, foregut, ears, nose and throat (ENT) or neurosurgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sudarshan R Jadcherla, MD
Organizational Affiliation
The Research Institute at Nationwide Children's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Reza Shaker, MD
Organizational Affiliation
Medical College of Wisconsin
Official's Role
Study Chair
Facility Information:
Facility Name
The Research Institute at Nationwide Children's Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43205
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19179881
Citation
Jadcherla SR, Stoner E, Gupta A, Bates DG, Fernandez S, Di Lorenzo C, Linscheid T. Evaluation and management of neonatal dysphagia: impact of pharyngoesophageal motility studies and multidisciplinary feeding strategy. J Pediatr Gastroenterol Nutr. 2009 Feb;48(2):186-92. doi: 10.1097/MPG.0b013e3181752ce7.
Results Reference
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PubMed Identifier
21694638
Citation
Jadcherla SR, Peng J, Moore R, Saavedra J, Shepherd E, Fernandez S, Erdman SH, DiLorenzo C. Impact of personalized feeding program in 100 NICU infants: pathophysiology-based approach for better outcomes. J Pediatr Gastroenterol Nutr. 2012 Jan;54(1):62-70. doi: 10.1097/MPG.0b013e3182288766.
Results Reference
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PubMed Identifier
18035137
Citation
Jadcherla SR, Gupta A, Stoner E, Fernandez S, Shaker R. Pharyngeal swallowing: defining pharyngeal and upper esophageal sphincter relationships in human neonates. J Pediatr. 2007 Dec;151(6):597-603. doi: 10.1016/j.jpeds.2007.04.042. Epub 2007 Aug 23.
Results Reference
background
PubMed Identifier
25279989
Citation
Jadcherla SR, Shubert TR, Gulati IK, Jensen PS, Wei L, Shaker R. Upper and lower esophageal sphincter kinetics are modified during maturation: effect of pharyngeal stimulus in premature infants. Pediatr Res. 2015 Jan;77(1-1):99-106. doi: 10.1038/pr.2014.147. Epub 2014 Oct 3.
Results Reference
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Mechanisms and Management of Infant Dysphagia

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