Efficacy and Safety of Alginos Oral Suspension to Treat Laryngopharyngeal Reflux

Laryngopharyngeal Reflux Clinical Trial

Official title:

A Double-blind, Randomized, Placebo-controlled Study to Evaluate the Efficacy and Safety of Alginos Oral Suspension (Sodium Alginate 50 mg/ml) for the Treatment of Patients With Laryngopharyngeal Reflux (LPR)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01450748
• Other study ID #: TTYALG1101
• Secondary ID: NTUH-IRB-2011060
• Status: Completed
• Phase: Phase 3
• First received: October 7, 2011
• Last updated: June 3, 2015
• Start date: October 2011
• Est. completion date: March 2015

Study information

• Verified date: June 2015
• Source: TTY Biopharm
• Contact: n/a
• Is FDA regulated: No
• Health authority: Taiwan: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

Laryngopharyngeal reflux (LPR), the backflow of gastric acid into the larynx and hypopharynx, is a contributing factor to hoarseness, throat clearing, throat pain, and globus sensation. The therapeutic effect of proton pump inhibitors (PPIs) is controversial because a high placebo effect can be observed. Sodium Alginate is an effective medication indicated for symptomatic treatment of gastroesophageal reflux. This randomized, double-blind, placebo-controlled study aims to evaluate the efficacy and safety profile of sodium alginates oral suspension (50 mg/ml) 20 ml 3 times daily for the treatment of with LPR patients in Taiwan. Efficacy assessments include mean reduction in the total reflux symptom index (RSI) score after 4 and 8 weeks treatment, mean reduction in the total reflux finding score (RFS) after 4 and 8 weeks treatment, mean changes in the total numbers of reflux episodes as measured by 24-hour ambulatory combined impedance-pH monitoring after 1 day and 8 weeks treatment. Safety assessments include incidence of adverse events. The study hypothesis is sodium alginate is superior over placebo in relieving LPR symptoms.

Description:

This double-blind, randomized, placebo-controlled trial aims to evaluate the efficacy and safety profiles of sodium alginate oral suspension (50mg/ml) 20ml 3 times daily for the treatment of patients with laryngopharyngeal reflux (LPR) in Taiwan. Patients will be enrolled into study if they are at the age of 12 to 75 years old, have at least one symptom consistent with LPR and lasting for more than 4 weeks before study, with a total reflux symptom index (RSI)>10, with a total reflux finding score (RFS)>5, and have signed the informed consent form. Patients will be excluded if they are diagnosed as erosive gastroesophageal reflux disease (GERD)as evidenced by upper GI endoscopy, viral or bacterial laryngitis, or occupational exposures causing laryngitis, laryngeal or hypopharyngeal cancer, esophageal or gastric cancer, with history of neck radiation therapy, with history of esophageal or gastric surgery, with active pulmonary infection (pneumonia, tuberculosis) as evidenced by chest X-ray, with endotracheal tube intubation within 2 months before entering study, or taking any alginate preparations within 2 days; H2-blocker, prokinetic agent or antacid within 7 days; or proton pump inhibitors (PPIs) within 14 days before screening. The primary efficacy endpoint is mean reduction in the total RSI from baseline to Week 8. The secondary efficacy endpoints are mean reduction in the total RSI from baseline to Day 2 and Week 4; mean reduction in the RFS from baseline to Week 4 and Week 8; mean change in the individual component of RSI from baseline to Day 2 , Week 4 and Week 8; mean change in the individual component of RFS from baseline to Week 4 and Week 8; and mean change in the total numbers of reflux episodes as measured by 24-hr ambulatory combined impedance-pH monitoring from baseline to day 2 and week 8. The safety endpoint is incidence of adverse events. The study hypothesis is that sodium alginate is superior over placebo in treating patients with LPR.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: March 2015
• Est. primary completion date: March 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 12 Years to 75 Years

Eligibility

Inclusion Criteria:

• Patients with age of 12-75 years old (inclusive)

• Patients with at least one symptom consistent with LPR, including hoarseness, throat clearing, throat pain, globus sensation in the throat, or chronic cough ? 4 weeks before entering study

• Patients with a total reflux symptom index (RSI) >10 (based on a self-administered 9-item questionnaire of voice/throat complaints)

• Patients with a total reflux finding score (RFS) >5 (based on a laryngoscopic examination by investigators)

• Patients or their legal representatives have signed the informed consent form

Exclusion Criteria:

• Patients with viral or bacterial laryngitis, or occupational exposures causing laryngitis

• Patients with erosive GERD as evidenced by upper GI endoscopy

• Patients with laryngeal or hypopharyngeal cancer, esophageal or gastric cancer, , or with history of neck radiation therapy

• Patients with history of uncontrolled hypertension or moderate to severe renal impairment

• Patients with history of esophageal or gastric surgery

• Patients with active pulmonary infection (pneumonia, tuberculosis) as evidenced by chest X-ray

• Patients with endotracheal tube intubation within 2 months before entering study

• Patients had taken any alginate preparations within 2 days; H2-blocker, prokinetic agent or antacid within 7 days; or proton pump inhibitors (PPIs) within 14 days before screening

• Patients with a history of allergy to the study drugs or their related compounds

• Patients with a history of alcohol or drug abuse, or with any psychiatric disease

• Patients participated any investigational drug trial within 4 weeks before entering the study

• Patients with any other conditions or diseases that investigator considers it is not appropriate to enter the study

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Gastroesophageal Reflux
• Laryngopharyngeal Reflux

Intervention

Drug:
• Sodium alginate
oral suspension, 50 mg/ml, 20 ml three times daily, 8 weeks
• Placebo
matching placebo oral suspension, 50 mg/ml, 20 ml three times daily, 8 weeks

Locations

Country	Name	City	State
Taiwan	TTY Biopharm Company Limited Taipei Branch	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
TTY Biopharm

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean reduction in the total reflux symptom index (RSI) score from baseline to Week 8	RSI is a self-administered 9-item questionnaire. RSI can be completed in less than 1 minute. The scale for each individual item ranges from 0 (no problem) to 5 (severe problem), with a maximum total score of 45. A total RSI score of >10 is suggestive of laryngopharyngeal reflux	before and after 8 weeks treatment	No
Secondary	Mean reduction in the total reflux symptom index (RSI) score from baseline to Day 2 and Week 4		before and after 1 day and 4 weeks treatment	No