To evaluate the effect and explore the mechanism of action behind the potential effect of Stretta® on GERD after SG.
Gastroesophageal reflux disease (GERD), i.e. the occurrence of troublesome symptoms or lesions as a consequence of retrograde flow of gastric contents into the esophagus, is one of the most prevalent gastrointestinal disorders. Obesity, defined by a body mass index (BMI) of ≥ 30 kg/m2, is an increasingly important problem in the Western world and a well-known risk factor for GERD related symptoms and esophagitis. Possible underlying mechanisms include an increased gastroesophageal pressure gradient, upward positional shift of the lower esophageal sphincter (LES) and increased occurrence of transient LES relaxations (TLESRs) after a meal. Bariatric surgery has emerged as a highly effective treatment for obesity and its associated metabolic complications. Roux-en-Y gastric bypass and sleeve gastrectomy (SG) currently account for the majority of the procedures. Several studies have reported improvement of GERD after gastric bypass and SG, probably through a combination of reduction of the acid-producing gastric mucosa and weight loss. However, in up to 34% of patients who underwent SG, de novo GERD or worsening of pre-existent GERD becomes evident, which established baseline GERD symptoms one of the few relative contra-indications for SG in many centers. Several post-operative alterations have been hypothesized to explain the increased incidence of GERD after SG: increased incidence of hiatal hernia due to the sleeve formation, dissection of the phreno-esophageal ligament, intrathoracic sleeve migration, increased intragastric pressure due to decreased gastric compliance and disruption of the competency of the esophagogastric junction (EGJ). Despite the fact that the majority of patients will respond to proton pump inhibitor (PPI) therapy, a significant proportion of patients continue to experience regurgitation and/or heartburn despite acid suppression although treatment outcome data are largely missing in the literature. These patients with refractory GERD symptoms after SG pose a challenge to surgeons and gastroenterologists since the postoperative anatomy does not allow classic fundoplication procedures. Stretta® (Mederi RF LLC, Houston TX, USA) is an endoscopic anti-reflux procedure using the delivery of radiofrequency energy to the LES. Stretta® is supported by the Society of American Gastrointestinal Endoscopic Surgeons (SAGES, ASGE and NICE) for the treatment of GERD in selected patients and is long-term cost-effective. Several controlled studies and a meta-analysis have reported improved symptoms after Stretta® although the effect on esophageal acid exposure time is inconsistent. Stretta® decreases the compliance of the EGJ without inducing fibrosis since the effect was reversed by administration of a nitric oxide donor and decreased sensitivity to distal acid perfusion. However, studies evaluating the symptomatic benefit of Stretta® in patients after SG are lacking, which is the primary goal of our study (primary endpoint). With the secondary endpoints, the effect of Stretta® will also be investigated on various aspects, which will provide an insight in the mechanism of action behind the potential effect of the intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
60
Annelies Geeraerts
Leuven, Belgium
RECRUITINGSymptom severity
Primary efficacy endpoint will be the change in symptom severity assessed by validated reflux questionnaires (ReQuest questionnaire and diaries) at week -1
Time frame: ReQuest questionnaire score will be assessed at week -1 after treatment
Symptom severity
Primary efficacy endpoint will be the change in symptom severity assessed by validated reflux questionnaires (ReQuest questionnaire and diaries) at week 12
Time frame: ReQuest questionnaire score will be assessed at week 12 after treatment
Symptom severity
Primary efficacy endpoint will be the change in symptom severity assessed by validated reflux questionnaires (ReQuest questionnaire and diaries) at week 24
Time frame: ReQuest questionnaire score will be assessed at week 24 after treatment
Symptom severity
Primary efficacy endpoint will be the change in symptom severity assessed by validated reflux questionnaires (ReQuest questionnaire and diaries) 1 year after treatment
Time frame: ReQuest questionnaire score will be assessed at 1 year after treatment
Objective reflux parameters
change in the objective reflux parameters on 24h pH-impedance (pH-MII) measurement
Time frame: Will be assessed week -1, week 12 and week 24
High Resolution impedance manometry
Change in HRiM paramters
Time frame: Will be assessed week -1 and week 24
EGJ distensibility (Endoflip)
Change in EGJ distensibility
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Time frame: Will be assessed week -1 and week 24
Esophageal sensitivity
Change in esophageal sensitivity
Time frame: Will be assessed week -1 and week 24
Esophageal permeability
Change in esophageal permeability assessed by transepithelial electrical resistance
Time frame: Will be assessed week -1 and week 24
Microscopic esophagitis (ESOHISTO score)
Change in esophagitis using esohisto scoring system
Time frame: Will be assessed week -1 and week 24