Gastro Esophageal Reflux Clinical Trial
Official title:
Antireflux Ablation Therapy (ARAT) With Hybrid-APC (Argon Plasma Coagulation) for GERD Treatment in Patients Without Hiatal Hernia
Gastroesophageal Reflux Disease (GERD) is defined as the rise of gastric or gastroduodenal contents above the esophagogastric junction (EGJ), generating symptoms and/or esophageal lesions. It is estimated a failure to treatment with PPI(proton pump inhibitor) between 10%-40% of patients with GERD. The main disadvantages of surgical treatment include perforation (0-4%), bleeding (<1%) and pneumothorax (0-10%), the most common late complication is gastric fullness, which occurs in almost all patients, approximately 25% of patients may experience persistent dysphagia 3 months after surgery and the most worrisome late complication is the need of a new surgical intervention. The aims of treatment at EGJ is to reduce gastroesophageal reflux contents into the esophagus. Hybrid-APC with ablation of EGJ (ARAT) is a new technique with could generate a scar remodeling this region and consequently reducing reflux disease. Our objective is to evaluate the safety and efficacy of ARAT in a group of patients with GERD without hiatal hernia.
Gastroesophageal reflux disease is a condition in which there is a rise of gastroduodenal
contents into the esophageal lumen, causing mucosal damage. Among treatments, medications are
the most common used ones but up to 10%-40% doesn't respond to this type of treatment.
Surgical treatment has been considered as the gold standard; however, with complications such
as bleeding, perforation, or dysphagia after surgery. Moreover, not all patients are
candidates to receive this type of treatment. Based on these data, new techniques have been
explored in order to reduce morbidity, mortality and costs in the treatment of these
patients.
Among different endoscopical treatments, ablation of EGJ is a new promising technique which
can be used to perform a closure at this level throughout the scar secondary to hybrid-APC
treatment, consequently decreasing gastroesophageal reflux. So, the aim of this study is to
evaluate safety and efficacy of ARAT in a group of patients with confirmed GERD.
This is a quasi experimental study that will be conducted in a tertiary care center in Mexico
city, Mexico. In an endoscopy department at the Mexican Institute of Social Security between
January 2018 and July 2019. Those patients diagnosed with gastroesophageal reflux who are
candidates and who accept this type of treatment will be evaluated. Patients who meet the
inclusion criteria will be the definitive candidates. The risks and benefits of this type of
endoscopic treatment will be explained as well as the potential scope of this endoscopic
alternative. We will evaluate safety and efficacy of this new procedure.
The technique of the procedure involves ablation of the mucosa of the EGJ using Hybrid-APC
(ARAT). The ablation field is initially marked with a Hybrid-APC. Subsequently, saline
solution mixed with indigo-carmine is injected at the submucosa level to raise a submucosal
bleb, followed by ablation of the mucosa along the lesser curvature. The approximate duration
of the procedure is 40min.
Follow-up will include objective evaluation of reflux disease with: upper endoscopy,
manometry, pHmetry, reflux questionnaire, and need of PPI (proton-pump inhibitor) dose
quantification.
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