Phase
Condition
Achalasia
Esophageal Disorders
Treatment
ValACYclovir 1000 MG
Shingrix
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male and female subjects aged 18-75 years old inclusive (females of childbearingpotential should be on highly effective contraceptive methods)
Fluent in English and mentally capable to provide informed consent who present toVanderbilt University Medical Center Digestive Diseases Center for treatment ofachalasia.
Based on standard clinical practice, we anticipate that patients who undergo thesetreatments will have been formally diagnosed with achalasia and will be fit toundergo the selected treatment intervention.
All subjects must be able to undergo timed barium swallow testing, trans-nasalintubation for high-resolution manometry probe, and therapeutic intervention of a 2-month course of valacyclovir 1g TID and two injections of Shingrix over atwo-month period.
Exclusion
Exclusion Criteria:
Unstable medical illness with ongoing diagnostic work-up and treatment. Patientswith well-controlled hypertension, diabetes and a remote history of ischemic heartdisease that is deemed stable, as judged by the physician-investigator can beincluded.
Current neurologic or cognitive impairment which would make the patient anunsuitable candidate for a research trial.
Study Design
Study Description
Connect with a study center
Vanderbilt University Medical Center
Nashville, Tennessee 37129
United StatesActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.