Efficacy and Safety of Sodium Alginate Oral Suspension to Treat Non-erosive Gastro-esophageal Reflux Disease

Phase

Condition

Heartburn

Esophageal Disorders

Heartburn (Pediatric)

Treatment

N/A

Clinical Study ID

NCT01338077

TTYALG1001

CGMH-IRB-99-1495A3

Ages 20-75
All Genders

Study Summary

About 60% of patients with typical gastroesophageal reflux symptoms such as heartburn and regurgitation are considered to have non-erosive reflux disease (NERD). Patients with NERD show an overall poorer response to PPI treatment than patients with erosive reflux disease. Sodium alginate oral suspension is a medication indicated for the relief of gastroesophageal reflux symptoms. This multi-center, double blind, randomized trial aims to compare the efficacy and safety profiles of sodium alginate oral suspension (50 mg/ml) 20 ml three times daily with that of omeprazole (20 mg/capsule) 1 capsule once daily for the treatment of NERD patients in Taiwan. Efficacy assessments include percentage of patients achieving adequate relief of heartburn or regurgitation after 4 weeks treatment, improvement of reflux symptoms as assessed by reflux disease questionnaire before and after treatment, and patients overall satisfaction at the end of study. Safety assessments include incidence of adverse events and change of the laboratory test results. The study hypothesis is that treatment with sodium alginate is non-inferior to omeprazole in relieving heartburn or regurgitation symptoms of the NERD patients.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Patients with age of 20-75 years old (inclusive) in Taiwan of both genders
Out-patients who had been diagnosed as non-erosive gastroesophageal reflux disease (NERD)
Patients with heartburn or regurgitation (either one) as main symptom at least 2 daysa week and had been present for > or = 1 month before screening
Patients with heartburn or regurgitation (either one) during the 7 days screeningperiod, either with frequency for > or = 4 days of mild symptom, or for > or = 2 daysof moderate to severe symptom
Patients have signed the informed consent form

Exclusion

Exclusion Criteria:

Patients with erosive gastroesophageal reflux disease (GERD), Barrett's esophagus oresophageal stricture
Patients with active or healing gastroduodenal ulcer (except scars)
Patients with history of gastric, duodenal or esophageal surgery
Patients with malignant disease of any kind
Patients with intrahepatic stone, gallstone, gallbladder sludge, hepatic or pancreaticcarcinoma as evidenced by abdominal ultrasonography
Patients with ischemic heart disease as evidenced by electrocardiogram
Female patients who are pregnant or nursing mother
Patients with a history of allergy to any of the study drugs or their relatedcompounds
Patients with a history of alcohol or drug abuse
Patients with clinically significant liver disease (aspartate aminotransferase (AST),alanine aminotransferase (ALT)>2 upper limits of normal)
Patients with clinically significant renal disease (serum creatinine >1.5 mg/dl)
Patients taken a proton pump inhibitor (PPI) within 14 days before screening, or aH2-blocker, prokinetic agent or antacid within 7 days before screening
Patients participated any investigational drug trial within 4 weeks before screening
Patients with any other conditions or diseases that investigator considers it is notappropriate to enter the study

Study Design

October 01, 2010

January 31, 2012

Study Description

This multi-center, double blind, randomized trial aims to compared the efficacy and safety profiles of sodium alginate oral suspension (50 mg/ml) 20 ml three times daily with that of omeprazole (20 mg/capsule) 1 capsule once daily for the treatment of non-erosive reflux disease (NERD) patients in Taiwan. Patients will be included into study if they are diagnosed as NERD; with heartburn or regurgitation (either one) as main symptom at least 2 days a week and had been present for ≧1 month before screening; with heartburn or regurgitation (either one) during the 7 days screening period, either with frequency for ≧4 days of mild symptom, or ≧ 2 days of moderate to severe symptom; and have signed the informed consent. Patients will be excluded if they are diagnosed as erosive gastroesophageal reflux disease (GERD), Barrett's esophagus or esophageal stricture; with active or healing gastroduodenal ulcer (except scars); with history of gastric, duodenal or esophageal surgery; with intrahepatic stone, gallstone, gallbladder sludge, hepatic or pancreatic carcinoma as evidenced by abdominal ultrasonography, with ischemic heart disease as evidenced by electrocardiogram; taking a proton pump inhibitor (PPI) within 14 days before screening, or a H2-blocker, prokinetic agent or antacid within 7 days before screening; or with clinically significant liver or kidney disease. The primary efficacy endpoint is percentage of patients achieving adequate heartburn (defined as a burning feeling or pain behind the breast bone) or regurgitation (defined as an acid taste in the mouth or unpleasant movement of material upwards from the stomach) relief at day 28 as assessed by patient diary. The secondary efficacy endpoints are percentage of patients achieving adequate heartburn or regurgitation relief at day 14; change from baseline of the reflux disease questionnaire total score at day 14 & 28; patients' overall satisfaction at the end of study; and number of antacid used during the 4-week treatment period. The safety endpoints are incidence of adverse events, and changes in laboratory test results (hematology, biochemistry, and urinalysis). The study hypothesis is that treatment with sodium alginate is non-inferior to omeprazole in relieving heartburn or regurgitation symptoms of the NERD patients.

Connect with a study center

Chang Gung Memorial Hospital
Taipei, 105
Taiwan
Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.