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Neonatal Gastro-Esophageal Reflux Disease (GERD) Management Trial (GMT)

Primary Purpose

Gastroesophageal Reflux Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Study Arm - acid suppression plus feeding bundle
Conventional arm - acid suppression only
Sponsored by
Sudarshan Jadcherla
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastroesophageal Reflux Disease focused on measuring infant, esophagitis, neonate, GERD

Eligibility Criteria

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

Inclusion Criteria:

  • Hospitalized infants with aerodigestive or GERD symptoms
  • Gestational age ≤42 weeks
  • Premature infants are eligible at 34 weeks postmenstrual age (PMA)
  • Enteral or Oral Fed
  • Average daily total feeding volume ≥ 150ml/kg/day
  • Room air or supplemental oxygen of ≤1 liter/minute (LPM) and/or ≤ 35% by nasal cannula

Exclusion Criteria:

  • Known genetic, metabolic or syndromic disease
  • Neurological diseases such as Grade 3 or 4 intraventricular hemorrhage (IVH) or intracranial hemorrhage (ICH) and perinatal asphyxia
  • Gastrointestinal malformations and surgical gastrointestinal conditions

Sites / Locations

  • The Research Institute at Nationwide Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Study

Conventional

Arm Description

Treated with omeprazole. This group of subjects will have prescribed restricted feeding volumes, monitored feeding duration time and positioning restrictions

Treated with omeprazole. This group of subjects will receive the current standard treatment for Gastro-esophageal reflux disease (GERD) which includes use of acid suppressive medication with no restrictions of the feeding volume, duration or positioning.

Outcomes

Primary Outcome Measures

CLINICAL OUTCOME OF FEEDING SUCCESS
The primary endpoint is the feeding success defined as achieving full oral feeds (defined as no need for tube feeds to maintain hydration and nutrition) and/or a >/= 6 point decrease from baseline symptom score as described by the Infant-Gastro-Esophageal Reflux Questionnaire-Revised. The minimum score is 0 (no symptoms) and the maximum score is 42 (maximum symptoms). Any total score greater than or equal to 16 is considered abnormal.
MOTILITY OUTCOMES: Presence of Esophageal Peristaltic Reflexes
This is part of Aim 2 of this RCT, which is a mechanistic outcome designed to understand the reasons for the clinical outcome. Presence of peristaltic reflex mechanisms elicited upon esophageal provocation during esophageal manometry were compared within the groups, week-5 vs. week-0. Odds ratios (ORs) with 95% confidence interval (CI) are reported from Generalized Estimation Equation models.

Secondary Outcome Measures

CLINICAL OUTCOMES: Growth Outcome Measure
Growth: The investigators will measure and track weight growth velocity during the study period
CLINICAL OUTCOME: Development Outcome Measures
Feeding Milestones: The investigators will track feeding method at 1 year.
CLINICAL OUTCOME: Respiratory Outcome Measures
Supplemental oxygen requirement at discharge was recorded for both groups

Full Information

First Posted
June 17, 2015
Last Updated
July 24, 2020
Sponsor
Sudarshan Jadcherla
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Ohio State University
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1. Study Identification

Unique Protocol Identification Number
NCT02486263
Brief Title
Neonatal Gastro-Esophageal Reflux Disease (GERD) Management Trial
Acronym
GMT
Official Title
Pathophysiology of the Aerodigestive Reflex in Infants: GERD Management Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
December 2012 (undefined)
Primary Completion Date
March 31, 2020 (Actual)
Study Completion Date
March 31, 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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The overall purpose of the investigator's study is to evaluate the causes of and treatment for feeding difficulty in infants with Gastro-esophageal Reflux Disease (GERD). New treatments can be possible only if the cause is known. Many infants have GERD and feeding difficulties, such as sucking and swallowing problems, vomiting, or delayed emptying of the stomach. Some of these infants have difficulty in protecting their airway during feeding or during reflux, and as a result can breathe fluid into their lungs or hold their breath. Most GERD treatments are done based on experience, but there is no scientific proof that these methods work for infants. GERD and feeding difficulties can lead to longer hospitalization and more stress for the family. In this clinical trial, the investigators are developing new methods to help with diagnosis as well as defining better treatment strategies in relieving GERD and GERD complications.
Detailed Description
Gastroesophageal reflux disease (GERD) and its troublesome complications constitute serious diagnostic and management challenges to the development of safe feeding and airway protection strategies among infants convalescing in the neonatal intensive care units; thus contributing to prolonged lengths of stay, recurrent hospitalizations, and death. GERD is frequently diagnosed by inadequate criteria, and the relative risks, benefits and indications of GERD therapies are unclear. Significant gaps in knowledge exist in understanding the complex causal or adaptive aerodigestive protective reflex mechanisms implicated in GERD in infants. The long-term goal is to improve digestive health, nutrition, and infant development through the design of simplified personalized treatment paradigms by better understanding the pathophysiology of aerodigestive reflexes. The current objective is to conduct a prospective single center randomized blinded controlled trial comparing the short term effects of the investigators innovative feeding strategy bundle (study approach) versus standard feeding approach (conventional approach).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux Disease
Keywords
infant, esophagitis, neonate, GERD

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
76 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study
Arm Type
Experimental
Arm Description
Treated with omeprazole. This group of subjects will have prescribed restricted feeding volumes, monitored feeding duration time and positioning restrictions
Arm Title
Conventional
Arm Type
Other
Arm Description
Treated with omeprazole. This group of subjects will receive the current standard treatment for Gastro-esophageal reflux disease (GERD) which includes use of acid suppressive medication with no restrictions of the feeding volume, duration or positioning.
Intervention Type
Other
Intervention Name(s)
Study Arm - acid suppression plus feeding bundle
Intervention Description
Omeprazole 0.5-1.5 milligrams/kilogram/dose twice a day (BID) Total fluid volume restriction (120-140 milliliters/kilogram/day) Feeding duration over 30 minutes Infant feeds with right side down Infant is placed on back following feeds
Intervention Type
Other
Intervention Name(s)
Conventional arm - acid suppression only
Intervention Description
-Omeprazole 0.5-1.5 milligrams/kilogram/dose twice a day (BID)
Primary Outcome Measure Information:
Title
CLINICAL OUTCOME OF FEEDING SUCCESS
Description
The primary endpoint is the feeding success defined as achieving full oral feeds (defined as no need for tube feeds to maintain hydration and nutrition) and/or a >/= 6 point decrease from baseline symptom score as described by the Infant-Gastro-Esophageal Reflux Questionnaire-Revised. The minimum score is 0 (no symptoms) and the maximum score is 42 (maximum symptoms). Any total score greater than or equal to 16 is considered abnormal.
Time Frame
Up to 5 weeks after enrollment
Title
MOTILITY OUTCOMES: Presence of Esophageal Peristaltic Reflexes
Description
This is part of Aim 2 of this RCT, which is a mechanistic outcome designed to understand the reasons for the clinical outcome. Presence of peristaltic reflex mechanisms elicited upon esophageal provocation during esophageal manometry were compared within the groups, week-5 vs. week-0. Odds ratios (ORs) with 95% confidence interval (CI) are reported from Generalized Estimation Equation models.
Time Frame
5 weeks
Secondary Outcome Measure Information:
Title
CLINICAL OUTCOMES: Growth Outcome Measure
Description
Growth: The investigators will measure and track weight growth velocity during the study period
Time Frame
at 5 weeks
Title
CLINICAL OUTCOME: Development Outcome Measures
Description
Feeding Milestones: The investigators will track feeding method at 1 year.
Time Frame
Up to 1 year age
Title
CLINICAL OUTCOME: Respiratory Outcome Measures
Description
Supplemental oxygen requirement at discharge was recorded for both groups
Time Frame
at discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
34 Weeks
Maximum Age & Unit of Time
60 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hospitalized infants with aerodigestive or GERD symptoms Gestational age ≤42 weeks Premature infants are eligible at 34 weeks postmenstrual age (PMA) Enteral or Oral Fed Average daily total feeding volume ≥ 150ml/kg/day Room air or supplemental oxygen of ≤1 liter/minute (LPM) and/or ≤ 35% by nasal cannula Exclusion Criteria: Known genetic, metabolic or syndromic disease Neurological diseases such as Grade 3 or 4 intraventricular hemorrhage (IVH) or intracranial hemorrhage (ICH) and perinatal asphyxia Gastrointestinal malformations and surgical gastrointestinal conditions
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
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
32380509
Citation
Jadcherla SR, Hasenstab KA, Wei L, Osborn EK, Viswanathan S, Gulati IK, Slaughter JL, Di Lorenzo C. Role of feeding strategy bundle with acid-suppressive therapy in infants with esophageal acid reflux exposure: a randomized controlled trial. Pediatr Res. 2021 Feb;89(3):645-652. doi: 10.1038/s41390-020-0932-4. Epub 2020 May 7.
Results Reference
background
PubMed Identifier
36310566
Citation
Sultana Z, Hasenstab KA, Moore RK, Osborn EK, Yildiz VO, Wei L, Slaughter JL, Jadcherla SR. Symptom Scores and pH-Impedance: Secondary Analysis of a Randomized Controlled Trial in Infants Treated for Gastroesophageal Reflux. Gastro Hep Adv. 2022;1(5):869-881. doi: 10.1016/j.gastha.2022.06.004. Epub 2022 Jun 20.
Results Reference
derived
PubMed Identifier
33259163
Citation
Jadcherla SR, Hasenstab KA, Gulati IK, Helmick R, Ipek H, Yildiz V, Wei L. Impact of Feeding Strategies With Acid Suppression on Esophageal Reflexes in Human Neonates With Gastroesophageal Reflux Disease: A Single-Blinded Randomized Clinical Trial. Clin Transl Gastroenterol. 2020 Nov;11(11):e00249. doi: 10.14309/ctg.0000000000000249.
Results Reference
derived

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Neonatal Gastro-Esophageal Reflux Disease (GERD) Management Trial

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