GERD
Conditions
Brief summary
Bodysurface gastric mapping (BSGM) will be used to assess gastric neuromuscular function in healthy controls and patients with medical refractory gastroesophageal reflux disease (GERD). Participants will undergo BSGM for 4-hours in addition to high resolution manometry (HRM), pH-impedance monitoring, and gastric emptying breath test.
Detailed description
This is a clinical trial of a non-invasive BSGM medical device (Gastric Alimetry) in patients with medical refractory GORD and healthy controls to determine the differences in gastric electrical activity, and correlate with adjacent measurements of gastro-esophageal function. Patients referred to the Functional Gut Clinic for standard care investigation of GORD with HRM and pH-impedance monitoring will be recruited. Healthy volunteers will be recruited via advertisement. All patients and healthy volunteers will undergo BSGM at the research site, which lasts around 4.5 hours. After a 0.5 hour baseline, subjects will undergo HRM and pH-impedance monitoring concomitantly. A test meal of porridge with C13 labelled octanoic acid will be consumed with BSGM and breath samples recorded for 4.0 hours after meal completion. The HRM catheter will be removed after 1.0 hour from finishing the test meal whist the pH-impedance monitoring will continue for the remainder of the site visit and for the remainder of the 24-hour study period whilst the subject is at home to quantify reflux.
Interventions
64-channel electrode array placed on the outer abdomen
Sponsors
The Functional Gut Clinic
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE
Intervention model description
Prospective, cross-sectional
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
Healthy controls Inclusion Criteria: * Aged 18-70 years old * BMI 18-35 * Able to understand written and spoken English * Able to provide written consent * Able to understand risks and benefits
Exclusion criteria
* Antacid use (e.g. PPI, H2RA or Gaviscon) within last 12-months * Active use of other medications known to impact gastric motility * Upper GI symptoms including but not limited to heartburn, regurgitation, epigastric pain, nausea and bloating * Significant medical condition * History of skin allergies or hypersensitivity * Active abdominal wounds or abrasions, fragile skin * Current pregnancy * Vulnerable group e.g. prisoners/cognitive impairment/institutionalised individuals * Regular cannabis users (unable to abstain for 7-days) * Opioid user * Unable to use a tablet device GORD patients Inclusion Criteria * Referred for 24-hour pH-impedance monitoring * Aged 18-70 years old * BMI 18-35 * Able to understand written and spoken English * Able to provide written consent * Able to understand risks and benefits
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Difference in BSGM parameters between GORD and healthy controls | 24-hours | Gastric Alimetry Rhythm Index (Normal \>0.25) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Correlate reflux event frequency with Gastric Alimetry Rhythm Index | 24-hours | Frequency of reflux events with Gastric Alimetry Rhythm Index |
| Correlate reflux event frequency with Prinicpal Gastric Frequency (cpm) | 24-hours | Frequency of reflux events with Prinicpal Gastric Frequency (cpm) |
| Correlate reflux event frequency with Fed:Fasted Amplitude ratio | 24-hours | Frequency of reflux events with Fed:Fasted Amplitude ratio |
| Correlate reflux event frequency with Average Amplitude | 24-hours | Frequency of reflux events with Average Amplitude (microvolts) |
| Correlate reflux event frequency with % of retrograde activity | 24-hours | Frequency of reflux events with % of retrograde activity |
| Correlate symptom severity with BSGM parameters | 24-hours | Real time discrete (vomiting, belching, reflux counts) and continuous (Nausea, bloating, upper gut pain, heartburn, stomach burn and excessive fullness) gastrointestinal symptom scores at both pre- and post-prandial time periods determined by a series of multiple 10-point symptom severity scales integrated within the validated Gastric Alimetry iOS Application with Gastric Alimetry Rhythm Index |
| Normal reference ranges for gastric emptying and BSGM | 24-hours | T lag and T 1/2 time (minutes) |
| Correlate the results of gastric emptying with BSGM parameters | 24-hours | T lag and T 1/2 (minutes) with ith Gastric Alimetry Rhythm Index |
| Correlate the results of oesophageal manometry with BSGM parameters | 24-hours | Distal contractile integral (mmHg.s.cm) with Gastric Alimetry Rhythm Index |
| Correlate the results of oesophageal manometry with Gastric Alimetry Rhythm Index | 24-hours | Integrated relaxation pressure (mmHg) with Gastric Alimetry Rhythm Index |
| Correlate the results of oesophageal manometry with Prinicpal Gastric Frequency | 24-hours | Integrated relaxation pressure (mmHg) with Prinicpal Gastric Frequency |
| Correlate the results of oesophageal manometry with % of retrograde activity | 24-hours | Frequency of transient lower oesophageal sphincter relaxation (TLOSRs) with % of retrograde activity |
| Correlate the results of hydrogen and methane breath testing with Gastric Alimetry Rhythm Index | 7 days | Total gas production (AUC ppm) with Gastric Alimetry Rhythm Index |
| Correlate quality of life with BSGM parameters | 24-hours | Total symptom burden scores according to the PAGI-QOL with Gastric Alimetry Rhythm Index |
Countries
United Kingdom
Contacts
Primary ContactAnthony Hobson, PhD
Outcome results
None listed