Abstract

BackgroundGastroesophageal reflux disease lowers the quality of life and increases medical costs. Electroacupuncture has been used to ease symptoms and improve gastrointestinal motility in patients with gastroesophageal reflux disease. The main purposes of this study are to evaluate the efficacy and safety of this procedure.Methods/designThis is a protocol for a randomized, patient-blinded, assessor-blinded, sham-controlled trial. Sixty participants with symptoms of gastroesophageal reflux disease, who have previously undergone standard treatment, will be recruited from August 2015 at Kyung Hee University Korean Medicine Hospital. The participants will be allocated to either the electroacupuncture (n = 30) or the sham electroacupuncture group (n = 30); the allocation will be concealed from both the participants and the assessors. The EA group will undergo penetrating acupuncture at 18 fixed points and two optional points chosen using the pattern identification for gastroesophageal reflux disease. Electrical stimulation will be applied at some of the acupoints. The sham electroacupuncture group will undergo nonpenetrating acupuncture without electrical stimulation at 18 nonspecific points, each of which will be only 2 cm away from the true acupoints used in the electroacupuncture group. In both groups, the procedure will be performed using the Park device. The treatment will last for 6 weeks (with two sessions each week), and the outcome will be evaluated at baseline, 3 weeks, and 6 weeks. The primary outcome will be the proportion of responders with adequate symptom relief, whereas the secondary outcomes will comprise the results of the Nepean dyspepsia index; the Korean gastrointestinal symptom rating scale; the EQ-5D™; levels of gastrin, motilin, and inflammatory cytokines; the perceived stress scale; the qi-stagnation questionnaire; the patient global impression of change; and the spleen qi deficiency questionnaire.DiscussionThe results of this trial will provide information about the efficacy and safety of electroacupuncture in the treatment of gastroesophageal reflux disease symptoms, as well as evidence regarding the use of electroacupuncture to treat gastroesophageal reflux disease in real clinical practice.Trial registrationClinical Research Information Service Identifier, KCT0001653. Registered on 12 October 2015.Electronic supplementary materialThe online version of this article (doi:10.1186/s13063-016-1371-8) contains supplementary material, which is available to authorized users.

Highlights

  • Gastroesophageal reflux disease lowers the quality of life and increases medical costs

  • The results of this trial will provide information about the efficacy and safety of electroacupuncture in the treatment of gastroesophageal reflux disease symptoms, as well as evidence regarding the use of electroacupuncture to treat gastroesophageal reflux disease in real clinical practice

  • If participants report adequate relief (AR) at more than half of all treatment sessions, they will be defined as responders, and we will compare the proportion of responders between the EA and sham EA groups

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Summary

Introduction

Gastroesophageal reflux disease lowers the quality of life and increases medical costs. Electroacupuncture has been used to ease symptoms and improve gastrointestinal motility in patients with gastroesophageal reflux disease. Approximately 20 % to 30 % of GERD patients continue to experience symptoms despite PPI treatment [6]. For this reason, interest is growing in complementary and alternative medicine—including acupuncture [5]. Acupuncture has been reported to possibly ease gastrointestinal symptoms [7] and improve esophageal motility [8]. According to several previous animal studies [9,10,11], electroacupuncture (EA) increases abnormally low esophageal sphincter pressure (ESP) and reduces the frequency of transient lower esophageal reflux relaxations (TLESRs); in so doing, the treatment increases esophageal motility. Little has been reported regarding the efficacy of EA in GERD; to our knowledge, no randomized controlled trials (RCTs), where a control group undergoes a sham procedure, have been carried out to evaluate the effect of EA on GERD in humans

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