Sleep Apnea Clinical Trial
Official title:
Effect of Continuous Positive Airway Pressure On Lower Esophageal Sphincter Pressure in Subjects Undergoing Bariatric Surgery
This trial is enrolling patients who are already being seen at OHSU weight loss clinic or
have been referred for clinical reasons by their physician to the OHSU weight loss clinic and
are going to have a esophageal manometry that would be paid for by their insurance company
for clinical reasons.
In patients undergoing weight loss surgery investigators plan to study the effect of
continuous positive airway pressure during a esophageal manometry.
Subjects will be invited to be in this research study because they are being considered for
weight loss (bariatric) surgery that is being paid for by their insurance company. As part of
the preparation for surgery, subjects will have a test called manometry that measures
pressure in the esophagus (food pipe). For this test, a tube will be lowered down one nostril
into the food pipe.
Studies have shown that Continuous Positive Airway Pressure (CPAP) reduces reflux in people
with or without sleep apnea as well as in people with reflux. The investigators are trying to
understand how this occurs. This research study will add about 10 additional minutes to the
clinic visit. The investigators expect about 50 subjects to be in the study at OHSU. Outcomes
will be measured at 18 months.
Patients scheduled for esophageal manometry and motility studies prior to their bariatric
surgery will be given a study flyer at the bariatric clinic. A list of the patients who are
interested in participating in the study will be given to one of the study investigators. A
study investigator will call these patients to explain the study, assess their interest in
participation, and review their eligibility for entrance into the study. Assessment of
eligibility will be done by asking for medical history over the phone as well as by
requesting access to their medical record to ensure the patients do not meet exclusion
criteria. After review of the patient's clinical history verbally and through review of the
medical record, informed consent will be signed at their manometry appointment.
Subjects will undergo the manometry procedure. After finishing the procedure, when the
catheter would normally be withdrawn after the procedure, it will remain in place for the
study. A CPAP mask will be placed over the subject's nose. CPAP blows air in the nose with a
mild pressure. The air pressure will be slowly increased while pressure in the esophagus is
being recorded. As done with the regular manometry, the subject will be asked to swallow
small amounts of water during the test. The test will be completed in 10 minutes. The CPAP
and the tube will be removed.
Subjects will complete a questionnaire prior to the manometry about gastrointestinal
symptoms.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05582070 -
Effect on Sleep of Surgical Treatment of Severe Nasal Obstruction
|
N/A | |
Recruiting |
NCT03919955 -
A Novel Pharmacological Therapy for Obstructive Sleep Apnea
|
Phase 2 | |
Completed |
NCT03927547 -
Sleep Disordered Breathing and Cardiopulmonary Disease in Peruvian Highlanders
|
N/A | |
Recruiting |
NCT04007380 -
Psychosocial, Cognitive, and Behavioral Consequences of Sleep-disordered Breathing After SCI
|
N/A | |
Completed |
NCT02188498 -
Electrocardiography Data Analysis in Sleep Disorders
|
||
Completed |
NCT01503164 -
Effects of Continuous Positive Airway Pressure (CPAP) on Glucose Metabolism
|
N/A | |
Recruiting |
NCT00747890 -
Surgical Treatment of Mild Obstructive Sleep Apnea
|
N/A | |
Active, not recruiting |
NCT00738179 -
Continuous Positive Airway Pressure Treatment of Obstructive Sleep Apnea to Prevent Cardiovascular Disease
|
Phase 3 | |
Completed |
NCT00841906 -
Alice PDx User/Validation Extended Trial
|
N/A | |
Completed |
NCT00202501 -
Usefulness of Nasal Continuous Positive Airway Pressure (CPAP) Treatment in Patients With a First Ever Stroke and Sleep Apnea Syndrome
|
N/A | |
Completed |
NCT00047463 -
Effects of Treating Obstructive Sleep Apnea in Epilepsy
|
Phase 2 | |
Not yet recruiting |
NCT06029881 -
Portable System for Non-intrusive Monitoring of Sleep
|
||
Recruiting |
NCT06093347 -
Central Apnoea Monitor Study
|
||
Terminated |
NCT05445869 -
Severe OSA Study (SOS)
|
N/A | |
Withdrawn |
NCT04096261 -
The Importance of Sleep Quality and the Blood-brain Barrier in Cognitive Disorders and Alzheimer's Disease
|
||
Recruiting |
NCT04575740 -
Phenotyping Mechanistic Pathways for Adverse Health Outcomes in Sleep Apnea
|
N/A | |
Completed |
NCT04676191 -
Validation of a Contactless Vital Signs Measurement Sensor
|
N/A | |
Recruiting |
NCT06015620 -
Comorbidities Resolution After MGB Surgery and Change in Body Composition
|
||
Completed |
NCT06051097 -
Metabolic Syndrome and Obstructive Sleep Apnea
|
||
Completed |
NCT05687097 -
Untreated Sleep Apnea as an Aggravating Factor for Other Secondary Medical Conditions After Spinal Cord Injury
|