Gastro Esophageal Reflux Disorder Clinical Trial
Official title:
Comparison of GERD and the Effects of Anti-Reflux Therapy on Pulmonary Function Between Able-Bodied and SCI Individuals
NCT number | NCT02584751 |
Other study ID # | RAD-16-02 |
Secondary ID | |
Status | Recruiting |
Phase | Phase 1 |
First received | October 9, 2015 |
Last updated | November 14, 2016 |
Start date | August 2016 |
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.
Status | Recruiting |
Enrollment | 110 |
Est. completion date | |
Est. primary completion date | August 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 75 Years |
Eligibility |
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 |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | James J. Peters VA Medical Center | Bronx | New York |
Lead Sponsor | Collaborator |
---|---|
James J. Peters Veterans Affairs Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | DeMeester Score | A DeMeester score will be calculated from the 24hour pH monitoring to determine if an individual has GERD. | 24hours | No |
Secondary | 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 | 2days | No |
Secondary | 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. | 2days | No |