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New treatment option for Gastroesophageal Reflux
Official title External UES Band (Shaker Pressure Band) and GERD
ClinicalTrials.gov ID: NCT05697393
What this study is testing
- What it's testing
- This protocol is a study to assess the efficacy of an external upper esophageal band to decrease subjective nighttime symptoms related to esophageal reflux into the pharynx.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 85
You may be able to join if
- The patient must be 18 years of age or older.
- Patients with gastroesophageal reflux disease (GERD) who has ear, nose, and throat symptoms, chronic cough, choking, or regurgitation (food coming...
- The patient has been diagnosed with GERD with extra-esophageal symptoms, esophagitis, hiatal hernia, achalasia, or diffuse esophageal spasm.
- The patient must not be pregnant or lactating.
You likely can't join if
- The patient cannot be younger than 18 years of age or older than 85.
- The patient cannot have sleep apnea or be on CPAP
- Patient cannot have previous head or neck surgery or radiation.
- Patient cannot have carotid artery disease, thyroid disease or history of cerebral vascular disease.
- Patients with an inability to tolerate nasal intubation.
- Patients with significant bleeding disorders for whom nasal intubation has been deemed contraindicated
See the full eligibility criteria
- The patient must be 18 years of age or older.
- Patients with gastroesophageal reflux disease (GERD) who has ear, nose, and throat symptoms, chronic cough, choking, or regurgitation (food coming back up into the throat).
- The patient has been diagnosed with GERD with extra-esophageal symptoms, esophagitis, hiatal hernia, achalasia, or diffuse esophageal spasm.
- The patient must not be pregnant or lactating.
- The patient cannot be younger than 18 years of age or older than 85.
- The patient cannot have sleep apnea or be on CPAP
- Patient cannot have previous head or neck surgery or radiation.
- Patient cannot have carotid artery disease, thyroid disease or history of cerebral vascular disease.
- Patients with an inability to tolerate nasal intubation.
- Patients with significant bleeding disorders for whom nasal intubation has been deemed contraindicated
- Patients with a known esophageal obstruction prevent passage of the manometry probe.
The study team makes the final eligibility decision.
Where it's taking place
- Milwaukee, Wisconsin, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 85 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Milwaukee, Wisconsin, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.