Gastro-esophageal Reflux Clinical Trial
Official title:
Pilot Study to Evaluate Esomeprazole (Nexium) in Treating Gastro-esophageal Reflux in Patients With Head and Neck Cancer With Prior External Beam Radiation Therapy: a Randomized, Prospective, Placebo-controlled, Double-blind Study.
Verified date | December 2017 |
Source | University of Iowa |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this research study is to measure acid reflux into the throat both before and
after medical treatment in people who have had radiation therapy to their head and neck for
the treatment of cancer. Many people who have received head and neck radiation therapy
develop a dry mouth as a result of the radiation damage to their saliva glands. In addition
to the discomfort associated with a dry mouth, the decrease in saliva may increase the
severity of gastro-esophageal reflux disease (acid reflux). Acid reflux occurs when acid
escapes from your stomach into your throat. You may not have any symptoms of acid reflux, but
often it can cause symptoms of heartburn or chest discomfort.
Acid reflux can be treated once it is diagnosed. Treatment consists of dietary changes,
behavioral alterations, and medication. Medications are available that decrease the amount of
acid in your stomach. Diagnosis of acid reflux is made with a pH-probe to test for acid in
your throat.
Status | Terminated |
Enrollment | 40 |
Est. completion date | February 2008 |
Est. primary completion date | October 2007 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Signed informed consent 2. History of head and neck cancer 3. Radiation Therapy (external beam or IMRT) 1. Must have received equal or greater than 5000 cGy cumulative dose 2. Must have complaint of xerostomia 3. Greater than three month interval since radiation treatment Exclusion Criteria: 1. Subjects unable to tolerate pH-probe in past 2. Subjects currently on proton-pump inhibitor (PPI) or H-2 receptor antagonist therapy 3. Prior history of esophago-gastric surgery 4. Symptoms of gastrointestinal bleeding (melena, hematemesis) 5. Known hepatic cirrhosis or esophageal varices 6. Prior esophageal perforation 7. Pregnant, nursing or not likely to be using adequate contraceptive measures 8. Subjects not predicted to survive duration of study 9. Subjects with allergies or sensitivities to proton-pump inhibitors 10. Psychological, familial, sociological or geographical conditions which do not permit Study follow-up and compliance with study protocol 11. Subjects predicted to undergo surgery, chemotherapy or radiation therapy for head and neck cancer during the course of study |
Country | Name | City | State |
---|---|---|---|
United States | University of Iowa Department of Otolaryngology | Iowa City | Iowa |
Lead Sponsor | Collaborator |
---|---|
Douglas Trask |
United States,
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