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Clinical efficacy of Yukgunja-tang combined with a proton pump inhibitor for refractory gastroesophageal reflux disease: study protocol for randomized, double-blind, double-dummy clinical trial.
Ha, Na-Yeon; Kim, Jung-Wook; Kim, Jinsung.
Afiliación
  • Ha NY; Department of Digestive Diseases, College of Korean Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.
  • Kim JW; Division of Digestive Diseases, Department of Korean Internal Medicine, Kyung Hee University Korean Medicine Hospital, Seoul, 02447, Republic of Korea.
  • Kim J; Division of Gastroenterology, Department of Internal Medicine, College of Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.
BMC Complement Med Ther ; 23(1): 444, 2023 Dec 07.
Article en En | MEDLINE | ID: mdl-38062418
ABSTRACT

BACKGROUND:

Yukgunja-tang (YGJ) is an herbal prescription used to treat the symptoms of gastroesophageal reflux disease (GERD). Although many preclinical and clinical studies on YGJ have been conducted on GERD, there is a lack of evidence from blinded studies to exclude placebo effects. Therefore, this protocol proposes a clinical trial that is single-centered, randomized, double-blinded, double-dummy to objectively evaluate the efficacy and safety of co-administered YGJ and rabeprazole (RPZ) in patients with GERD previously treated with proton pump inhibitors (PPIs) and still experiencing symptoms.

METHODS:

A total of 86 participants with refractory GERD (rGERD) will be randomized in a 11 ratio to the treatment [YGJ and RPZ (10 mg/d)] and control groups [double-dose RPZ (20 mg/d)] for 4 weeks of treatment (weeks 0-4) followed by 4 weeks of follow-up (weeks 4-8). The Frequency Scale for the Symptoms of GERD will be analyzed for the primary endpoint. Reflux Disease Questionnaire, Reflux Symptom Score, GERD-Health Related Quality of Life, Overall Treatment Evaluation, Spleen Qi Deficiency Questionnaire, Damum Questionnaire, and dyspepsia Visual Analogue Scale will be used to evaluate treatment effects on GERD related symptoms and quality of life and to compare treatment effects by subgroups. Safety tests will be analyzed by investigating adverse events.

DISCUSSION:

This clinical trial will be the first rigorous double-blind, double-dummy, placebo-controlled study to precisely evaluate the efficacy and safety of the combination of YGJ and PPIs in the treatment of rGERD. The results of this study will provide a reliable clinical basis for selecting botanical drug treatments for patients with rGERD. TRIAL REGISTRATION Clinical Research Information Service (registration number KCT0008600, July 13, 2023, https//cris.nih.go.kr ).
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Reflujo Gastroesofágico / Inhibidores de la Bomba de Protones Idioma: En Revista: BMC Complement Med Ther Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Reflujo Gastroesofágico / Inhibidores de la Bomba de Protones Idioma: En Revista: BMC Complement Med Ther Año: 2023 Tipo del documento: Article