search
Back to results

GERD and Anti-Reflux Therapy Between Able-bodied and SCI Individuals

Primary Purpose

Gastro Esophageal Reflux Disorder

Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Omeprazole
24 Hour pH Monitor
Pulmonary Function Examination
Exhaled Nitric Oxide
Exhaled Breath Concentrate (EBC)
Bernstein's Acid Clearance Test
Esophageal Motility
Sponsored by
James J. Peters Veterans Affairs Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastro Esophageal Reflux Disorder

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Subjects with Tetraplegia (Level of SCI C4-8);
  • Subjects with High Paraplegia (Level of SCI T1-T7);
  • Subjects with Low Paraplegia (Level of SCI T8 or below);
  • Able-Bodied Subjects (non SCI)
  • Duration of injury ≥ 1 year; and
  • Chronological age between 18-75 years.

Exclusion Criteria:

  • Smoking, active or history of smoking < 6 months;
  • Any history of blast injuries to the chest;
  • Active respiratory disease or recent (within 3 months) respiratory infections;
  • Use of medications known to alter airway caliber (i.e. beta 2 agonists or anticholinergic agents);
  • Use of Protein Pump Inhibitors < 8 weeks before testing;
  • Use of H2 receptor blockers <8 weeks before testing;
  • History of gastrectomy;
  • History of esophageal malignancy and/or resection

Sites / Locations

  • James J. Peters VA Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Experimental

Active Comparator

Arm Label

Able-Bodied non-GERD

SCI non-GERD

SCI GERD

Able-bodied GERD

Arm Description

Able-bodied patients who are not diagnosed with GERD during screening will act as controls.

SCI patients who are not diagnosed with GERD during screening will act as controls

For those SCI subjects who are identified with GERD, they will undergo a 8week treatment of Omeprazole to reduce GERD

For those AB subjects who are identified with GERD will act as controls. Note they will not receive treatment for GERD in this study. We will notify their primary care physician during the study so that they may receive treatment.

Outcomes

Primary Outcome Measures

DeMeester Score
A DeMeester score will be calculated from the 24hour pH monitoring to determine if an individual has GERD.

Secondary Outcome Measures

Pulmonary Function Tests
Pulmonary Function values and results will be compared to one another to determine if a protein pump inhibitor treatment decreases GERD and improves pulmonary function
Symptom Surveys and Questionnaires
An 11 question survey assessing GERD and a 15 question survey assessing dysphagia or difficulty swallowing will be used to confirm diagnosis of GERD and compared across the various groups.

Full Information

First Posted
October 9, 2015
Last Updated
November 14, 2016
Sponsor
James J. Peters Veterans Affairs Medical Center
search

1. Study Identification

Unique Protocol Identification Number
NCT02584751
Brief Title
GERD and Anti-Reflux Therapy Between Able-bodied and SCI Individuals
Official Title
Comparison of GERD and the Effects of Anti-Reflux Therapy on Pulmonary Function Between Able-Bodied and SCI Individuals
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
August 2016 (undefined)
Primary Completion Date
August 2018 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
James J. Peters Veterans Affairs Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Respiratory dysfunction, esophageal dysmotility, and a gastroesophageal reflux disease (GERD) have been demonstrated to be highly prevalent in persons with SCI. GERD has been linked to respiratory symptoms and conditions such as asthma, chronic cough, and an increased rate of respiratory infections in the general population. In persons with asthma, respiratory symptoms and dependency on asthma medications have been reduced by treatment with anti-reflux medication. Possible mechanisms have been proposed for this link, including the microaspiration of reflux materials, which may result in airway acidification and aspiration pneumonia, or the stimulation of the vagus nerve through acid-sensitive receptors in the esophagus with associated esophageal inflammation and reflex bronchoconstriction. Investigators propose to study the effects of anti-reflux therapy (proton pump inhibition) in persons with SCI on objective and subjective symptoms of respiratory function to determine the underlying mechanisms of airway inflammation due to GERD.
Detailed Description
Complete or partial loss of respiratory muscle innervation in individuals with cervical (C1-8) and high thoracic (T1-6) injuries leads to inadequate ventilation and inability to effectively clear secretions, often prompting supportive ventilation following initial injury. Development of atelectasis, pneumonias and respiratory failure are the most common respiratory complications observed during the acute phase of injury. The role of chronic airway inflammation on pulmonary function in persons with SCI is unknown, although the investigators' recent work has shown that individuals with cervical SCI have elevated levels of exhaled nitric oxide (NO), comparable to those seen in mild asthma. It is now widely believed that in the airways of asthmatic patients, the release of NO represents a physiological mechanism to counteract the bronchoconstriction caused by various stimuli. In persons with cervical SCI, bronchoconstriction may represent a consequence of unopposed parasympathetic influence, but alternative mechanisms, such as recurrent infections secondary to impaired cough effectiveness, systemic inflammatory response following SCI, or extra-esophageal manifestations of underlying esophageal dysmotility and/or GERD need to be evaluated. In general population, it has been long recognized that esophageal dysmotility and/or GERD may lead to extra-esophageal manifestations. Reflux can affect both upper and lower respiratory systems leading to the variety of extra-esophageal manifestations, such as reflux asthma, chronic cough, hoarseness, chronic sinusitis, laryngitis, loss of dental enamel, idiopathic pulmonary fibrosis, recurrent pneumonia, chronic bronchitis, etc. 2 possible mechanisms of these complications have been identified: the direct aspiration of reflux content and indirectly, stimulation of vagally-mediated reflexes. Regardless of the underlying mechanisms, treatments with acid-reducing therapies have shown improvement in GERD and extra-esophageal manifestations of the disease the general population. Investigators propose to study the effects of anti-reflux therapy (proton pump inhibition) in persons with SCI on objective and subjective symptoms of respiratory function to determine the underlying mechanisms of airway inflammation due to GERD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastro Esophageal Reflux Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
110 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Able-Bodied non-GERD
Arm Type
Active Comparator
Arm Description
Able-bodied patients who are not diagnosed with GERD during screening will act as controls.
Arm Title
SCI non-GERD
Arm Type
Active Comparator
Arm Description
SCI patients who are not diagnosed with GERD during screening will act as controls
Arm Title
SCI GERD
Arm Type
Experimental
Arm Description
For those SCI subjects who are identified with GERD, they will undergo a 8week treatment of Omeprazole to reduce GERD
Arm Title
Able-bodied GERD
Arm Type
Active Comparator
Arm Description
For those AB subjects who are identified with GERD will act as controls. Note they will not receive treatment for GERD in this study. We will notify their primary care physician during the study so that they may receive treatment.
Intervention Type
Drug
Intervention Name(s)
Omeprazole
Intervention Description
Omeprazole is a commonly prescribed anti-reflux medication. If a SCI patient has GERD, they will be prescribed with 40mg omeprazole twice daily for two months
Intervention Type
Device
Intervention Name(s)
24 Hour pH Monitor
Intervention Description
Monitors the acidity and levels of pH in the esophagus for 24hours and helps diagnose people with GERD
Intervention Type
Procedure
Intervention Name(s)
Pulmonary Function Examination
Intervention Description
Assess pulmonary function such as lung volumes, spirometry, and max inspiration/expiration pressures.
Intervention Type
Procedure
Intervention Name(s)
Exhaled Nitric Oxide
Intervention Description
Used to measure inflammation markers for airway resistance.
Intervention Type
Procedure
Intervention Name(s)
Exhaled Breath Concentrate (EBC)
Intervention Description
EBC will be used to measure airway inflammation via specific markers, such as 8-isoprostane. This marker, if elevated, has been identified as an indicator for asthma inflammation.
Intervention Type
Procedure
Intervention Name(s)
Bernstein's Acid Clearance Test
Intervention Description
Bernstein test is a clinical test for the diagnosis of chest pain in association with gastric acid exposure
Intervention Type
Procedure
Intervention Name(s)
Esophageal Motility
Intervention Description
Esophageal Motility will be used to measure a subject's ability to swallow a bolus (i.e. saline solution) and record pressure changes throughout the esophagus during the swallow. This will also be used to identify anatomical landmarks, such as lower esophageal sphincter, which are necessary for proper placement of 24hr pH catheter.
Primary Outcome Measure Information:
Title
DeMeester Score
Description
A DeMeester score will be calculated from the 24hour pH monitoring to determine if an individual has GERD.
Time Frame
24hours
Secondary Outcome Measure Information:
Title
Pulmonary Function Tests
Description
Pulmonary Function values and results will be compared to one another to determine if a protein pump inhibitor treatment decreases GERD and improves pulmonary function
Time Frame
2days
Title
Symptom Surveys and Questionnaires
Description
An 11 question survey assessing GERD and a 15 question survey assessing dysphagia or difficulty swallowing will be used to confirm diagnosis of GERD and compared across the various groups.
Time Frame
2days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects with Tetraplegia (Level of SCI C4-8); Subjects with High Paraplegia (Level of SCI T1-T7); Subjects with Low Paraplegia (Level of SCI T8 or below); Able-Bodied Subjects (non SCI) Duration of injury ≥ 1 year; and Chronological age between 18-75 years. Exclusion Criteria: Smoking, active or history of smoking < 6 months; Any history of blast injuries to the chest; Active respiratory disease or recent (within 3 months) respiratory infections; Use of medications known to alter airway caliber (i.e. beta 2 agonists or anticholinergic agents); Use of Protein Pump Inhibitors < 8 weeks before testing; Use of H2 receptor blockers <8 weeks before testing; History of gastrectomy; History of esophageal malignancy and/or resection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Miroslav Radulovic, MD
Phone
718-584-9000
Ext
5472
Email
miroslav.radulovic@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Tradd Cummings, MS
Phone
718-584-9000
Ext
3107
Email
tradd.cummings@va.gov
Facility Information:
Facility Name
James J. Peters VA Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10468
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tradd Cummings, MS
Phone
718-584-9000
Ext
3107
Email
tradd.cummings@va.gov
First Name & Middle Initial & Last Name & Degree
Josh Hobson, MS
Phone
(718) 584-9000
Ext
3129
Email
joshua.hobson@va.gov
First Name & Middle Initial & Last Name & Degree
Mark A Korsten, MD
First Name & Middle Initial & Last Name & Degree
Miroslav Radulovic, MD
First Name & Middle Initial & Last Name & Degree
Marinella D. Galea, MD
First Name & Middle Initial & Last Name & Degree
Gregory Schilero, MD

12. IPD Sharing Statement

Learn more about this trial

GERD and Anti-Reflux Therapy Between Able-bodied and SCI Individuals

We'll reach out to this number within 24 hrs