Skip to main content
Clinical Trials/NCT01822106
NCT01822106
Unknown
Phase 4

Randomized, Double Blind, Placebo Control Trial to Evaluate the Efficacy of Wu-Chu-Yu Tang on Gastroesophageal Reflux Disease (GERD)

China Medical University Hospital1 site in 1 country90 target enrollmentFebruary 2013

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Gastroesophageal Reflux Disease
Sponsor
China Medical University Hospital
Enrollment
90
Locations
1
Primary Endpoint
RDQ Questionnaire
Last Updated
13 years ago

Overview

Brief Summary

GERD is due to gastric content reflux to esophagus cause symptom and complication including intra-esophagus such as reflux esophagitis, and extra-esophagus such as cough etc. Because the changes of dietary habit, and improvement of examination skill and data analysis, the prevalence of GERD increased 2.5 multiple from 1995 to 2002, and suggesting the prevalence is 25% in Taiwan community.

Although proton pump inhibitor (PPI) can inhibit gastric acid secretion, relief symptom and enhancing repair of esophageal damage, therefore, PPI is a main drug for the treatment of GRED, but because of PPI has disadvantage of poor compliance, and slow gastric empty time and hypersensitivity, and about 40-50% of GERD patients is inefficacy. In addition, PPI produces bone fracture, community pneumonia and diarrhea in patient with long-term use.

Wu-Chu-Yu tang consists of Evodia fargesii Dode (Evodia Fruit), Panax ginseng C. (Ginseng), Ziziphus jujube Mill (Chinses Date), Zingiber officinale Rosee (Fresh Ginger). According to "I-Fang-Chi-Chieh" and "Shanghonzobinglun" recordings that Wu-Chu-Yu tang can treat vomiting, and also can relax gastric tonicity and can enhance peristalsis of stomach.

Therefore, the purpose of the present study was to investigate the efficacy of Wu-Chu-Yu tang on GRED, and this effect of Wu-Chu-Yu tang compared to PPI Omeprazole.

Registry
clinicaltrials.gov
Start Date
February 2013
End Date
December 2014
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Gender:Male or female.
  • Age: from 20 y/o to 75 y/o.
  • The diagnosis is Gastroesophageal Reflux Disease.
  • With the symptoms of heartburn or acid regurgitation.
  • After explaining thoroughly the whole research purpose or process, the clients are willing to sign the agreement.

Exclusion Criteria

  • Exclude peptic ulcer, gall bladder stone (including intraheptaic and common hepatical duct) and major diseased of cancer.
  • Barrett's esophagus or esophagus stricture.
  • The operation history of esophagus or gastroduodenoal regions.
  • Tarry stool suspected GI tract bleeding.
  • With the history of alcohol or drug abuse.
  • The clients with the history of study drug allergy.
  • The clients with psychologic cannot cooperate with each other.
  • The pregnant woman or the lactating women.
  • Abnormal liver function such as GOT, GPT elevated over double the normal range.

Outcomes

Primary Outcomes

RDQ Questionnaire

Time Frame: Chang from baseline RDQ score at week 4 (28 ± 5 days)

Secondary Outcomes

  • GerD Questionnaire(Chang from baseline GerD score at week 4 (28 ± 5 days))

Study Sites (1)

Loading locations...

Similar Trials