GERD and Anti-Reflux Therapy Between Able-bodied and SCI Individuals
Gastro Esophageal Reflux Disorder
About this trial
This is an interventional treatment trial for Gastro Esophageal Reflux Disorder
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
Sites / Locations
- James J. Peters VA Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Active Comparator
Experimental
Active Comparator
Able-Bodied non-GERD
SCI non-GERD
SCI GERD
Able-bodied GERD
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.