MULTICENTER SINGLE-BLIND RANDOMIZED CONTROLLED TRIAL OF LAPAROSCOPIC PARAESOPHAGEAL HIATAL HERNIA REPAIR COMBINED WITH TRANSORAL INCISIONLESS FUNDOPLICATION VERSUS LAPAROSCOPIC NISSEN FUNDOPLICATION FOR TREATMENT OF GASTROESOPHAGEAL REFLUX DISEASE IN PATIENTS REQUIRING HIATAL HERNIA REPAIR
Follow the link to read more about the study: https://clinicaltrials.gov/ct2/show/NCT04795934?recrs=a&cond=GERD&cntry=US&state=US%3ACO&draw=2&rank=2
LINX WITH HIATAL HERNIA
Institute of Esophageal and Reflux Surgery is now enrolling patients for this study. We are participating in a multi-center study to look at the use of the LINX Reflux Management System in patients with moderate sized hiatal hernias. We are again the only site in the Rocky Mountain Region to be able to offer this study. Follow link to learn more:
RETHINK REFLUX REGISTRY, RESEARCH TO FURTHER INFORM THINKING ABOUT THE ROLE OF LINX FOR REFLUX DISEASE
Active, no longer recruiting.
Now closed. We are the first site in the country and the only site in the Rocky Mountain region to start enrolling patients in the CALIBER study which is a randomized study look at the LINX device compared to taking reflux medications. We enrolled more than any other site in the country. Results to be published soon….
This is a randomized placebo controlled trial to look at the efficacy of the Esophyx device. This study is now closed. Click below to read the results.
This is an ongoing evaluation of patients that have had the Esophyx/TIF procedure to see how they are doing long term. This study is now closed.
LINX post market analysis
We are the only site in the Rocky Mountain Region that was asked to participate in a study to evaluate patients long term who have had the LINX device placed. This is a requirement by the FDA after approving the device for use. This study is now closed.
Prospective study- This is an ongoing study to evaluate all aspects of our care, from testing and diagnosis to outcomes of surgery. By carefully evaluating our data, we are able to improve outcomes, establish quality control, and publish our information.
The purpose of the study is to collect information about the use of the LINX device in patients who have previously undergone a Laparoscopic Sleeve Gastrectomy (LSG). Like other patients with a weak lower esophageal sphincter (LES), post-LSG patients may remain susceptible to gastroesophageal reflux disease (GERD) until the LES barrier function is restored. However, post-LSG patients have limited options for reflux control given their altered gastric anatomy which may not allow them to have standard surgical anti-reflux procedures like fundoplication. The safety and effectiveness of the LINX device has not been established in patients with a previous LSG.
If you are interested in learning more about our studies email Rachel at firstname.lastname@example.org or call 303-788-7700 opt 3.
To see all publications, click here.