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OpenTrials
Completed

NCT Number: NCT02972047

Understanding the Pathophysiology and Effects of Diaphragmatic Breathing in Upright Gastroesophageal Reflux

This study aims to understand why patients have predominantly upright gastroesophageal reflux disease by comparing such patients to healthy persons AND whether a behavioral intervention (diaphragmatic breathing) will impact this disease

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic in Rochester

Rochester, Minnesota, 55905, United States

About this study

There are two major patterns of gastroesophageal reflux disease (GERD), predominantly daytime and upright reflux and predominantly nocturnal and supine reflux.

Traditionally, upright reflux has been attributed to more frequent or wider opening with transient lower esophageal sphincter relaxations (TLESRs) while supine reflux results from a consistently reduced lower esophageal sphincter (LES) pressure. This may further be accounted for by the finding of larger hiatal hernias and greater pressure gradients between the crura and LES when comparing supine to upright refluxers. These findings may help explain supine reflux, but they offer little insight into the mechanisms of upright reflux.

In this study the investigators will be recruiting twenty healthy persons and up to 60 patients with GERD will be recruited from the clinical practice at Mayo Clinic Rochester. The investigators aim to study the intervention on 40 patients with GERD. However, recognizing that up to 33% of patients with typical symptoms of GERD will not have reflux by ambulatory pH monitoring (pH power of hydration), the investigators provide for enrolling up to a maximum of 60 patients which should be sufficient to yield 40 patients with upright GERD by pH monitoring. In addition, up to 10 additional healthy persons may be recruited.

Subjects with upright reflux and healthy controls will be randomized into one of two groups:

Experimental: Diaphragmatic breathing or Sham comparator: (listening to music/watching Television (TV) for 30 minutes after each meal to see how this impacts the disease.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for Healthy Persons:

-Patients 18 years of age or older with no symptoms of GERD

Inclusion criteria

for Patients:

  • Patients 18 years of age or older with symptoms of GERD
  • Upper gastrointestinal endoscopy within the past 6 months and a prior diagnostic pH impedance study showing predominantly upright reflux

Exclusion criteria

for Patients; Items indicated with an asterisk (*) are also exclusion criteria for healthy persons

  • Patient who fulfil ROME IV Criteria for rumination disorder20
  • Clinical evidence of significant cardiovascular, respiratory, renal, hepatic, gastrointestinal, hematological, neurological (e.g., spinal cord injuries, dementia, multiple sclerosis, Parkinson's disease), psychiatric or other disease that may interfere with the objectives of the study and/or pose safety concerns.*
  • Any prior gastric or esophageal surgery and significant intestinal or colonic resection*
  • Hiatal hernia measuring 3 cm or larger as assessed by endoscopic or radiological studies
  • Prior history of Los Angeles Grade C or D esophagitis, or esophageal stricture.
  • Current use opioid analgesics or anticholinergic drugs.* We will permit low doses of tricyclic antidepressants, nortriptyline (up to 50 mg/day) or amitriptyline (up to 25 mg/day) provided they were commenced 3 months prior to the screening period, calcium channel or adrenergic1 antagonists
  • Current use of proton pump inhibitors
  • Known significant esophageal motor disorder (ie achalasia, aperistalsis, functional obstruction, jackhammer, distal esophageal spasm)*
  • Inability to read due to: blindness, cognitive dysfunction, or English language illiteracy *
  • Pregnant and lactating females *

Exclusion criteria

for Healthy Persons in addition to those marked with an Asterisk (*) above

  • Ongoing use of Proton Pump Inhibitors ( PPIs) or a history consistent with GE reflux for 3 months or longer duration in past.
  • Prior history of Los Angeles Grade B-D esophagitis
  • Prior history of GERD on the basis of pH testing

Treatment and study plan

Diaphragmatic breathing

Behavioral

Subjects in this are practice diaphragmatic breathing for 30 minutes after each meal.

Sham Comparator

Behavioral

Sham therapy (listening to music/watching TV for 30 minutes after each meal

Primary outcomes

  1. The total esophageal acid exposure time during the diagnostic 24hour pH study compared with the interventional study

    Time frame: 2 days

    The investigators will compare the total esophageal acid exposure time in minutes during the first 24 hour ambulatory pH study with the second 24 period during which patients are either randomized to biofeedback versus sham

Secondary outcomes

  1. Upper gastrointestinal pressures in patients with upright GER compared to healthy people

    Time frame: 2 days

    Upper gastrointestinal pressures and pressure changes associated with meals will be described. Pressure differences will be measured in mmHg.

  2. The effects of provocative maneuvers on upper gastrointestinal pressures.

    Time frame: 2 days

    The investigators will compare the effects of provocative maneuvers on upper gastrointestinal pressure. Pressure differences will be measured in mmHg.

  3. The effects of provocative maneuvers on reflux

    Time frame: 2 days

    The investigators will compare the effects of provocative maneuvers on reflux as measured with impedance (Ohms)

  4. The effects of diaphragmatic breathing on upper gastrointestinal pressures

    Time frame: 2 days

    The investigators will report any pressure changes (measures in mmHg) associated with diaphragmatic breathing on upper gastrointestinal pressure.

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Important dates

Study start
2017
Primary completion
2020
Study completion
2020
First posted
Nov 23, 2016
Registry last updated
Dec 4, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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