Dysphagia Clinical Trial
Official title:
Prospective Study to Assess the Diagnostic Utility of Amyl Nitrite in Patients With Suspected Achalasia Undergoing High Resolution Esophageal Manometry (HREM)
NCT number | NCT02428959 |
Other study ID # | IRB00029912 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2014 |
Est. completion date | December 2018 |
Verified date | September 2019 |
Source | Johns Hopkins University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This research is being done to see if a study drug called amyl nitrite can be helpful with
diagnosing different disorders affecting the lower esophageal sphincter in patients with
dysphagia (difficulty swallowing foods) undergoing high resolution esophageal manometry
(HRM).
Dysphagia may be one of the symptoms of a condition known as idiopathic achalasia. Achalasia
is a disorder of the esophagus, the tube that carries food from the mouth to the stomach.
This affects the ability of the esophagus to move food toward the stomach. Pseudoachalasia is
a secondary form of achalasia, which has very similar symptoms but is caused by different
reasons. Because the treatments for achalasia and pseudoachalasia are different, it is
important to correctly diagnose each condition. At this time, there is no way to distinguish
the two with the current tests used at Johns Hopkins.
Amyl nitrite relaxes vascular smooth muscle and has been studied previously as a potential
means to separate achalasia from pseudoachalasia. Amyl nitrite is approved by the Food and
Drug Administration (FDA) for the treatment of cardiac angina. It is not approved for use in
motility testing and its use in this study is considered investigational. Investigators hope
that the results from the proposed study could have significant clinical implications for
patient management by helping doctors distinguish between achalasia and pseudoachalasia and
allow them to choose appropriate treatment.
Patients with dysphagia (difficulty swallowing foods) undergoing routinely scheduled high
resolution esophageal manometry (HRM) may join this study.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2018 |
Est. primary completion date | December 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - age 18-80 years old - symptoms of dysphagia or a known history of achalasia Exclusion Criteria: - Patients with comorbidity and contraindications to use of amyl nitrite inhalation: Glaucoma, Recent head trauma or cerebral hemorrhage, Hypotension, Concurrent use of nitrite, Pregnancy, Aortic stenosis, Patients with increased intracranial pressure, Caution in patients with coronary artery disease, Pulmonary hypertension - Non-English speakers - Patients <18 years old - Those who lack capacity to give consent |
Country | Name | City | State |
---|---|---|---|
United States | Johns Hopkins Hospital | Baltimore | Maryland |
Lead Sponsor | Collaborator |
---|---|
Johns Hopkins University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Measure LES pressure after amyl nitrite inhalation in patients with dysphagia undergoing high resolution esophageal manometry (HRM) | 3 months | ||
Secondary | Measure Blood Pressure and Heart Rate at baseline and after administration of amyl nitrite | 1 month | ||
Secondary | Number of Participants with Adverse Events with amyl nitrite inhalation | 1 month |
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