MedTrace Logo

Efficacy and Safety of InSan Bamboo Salt on Improvement of Helicobacter Pylori Infection

NCT01735136 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2019-08-26

No results posted yet for this study

Summary

The investigators performed a 4-week, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of InSan Bamboo Salt on improvement of Helicobacter pylori infection. The investigators measured improvement of Helicobacter pylori infection parameters , including 14C-UBT(Urea breath test), and subjects' symptoms, and monitored their blood pressure.

Conditions

  • Helicobacter Pylori Infection

Interventions

DIETARY_SUPPLEMENT

InSan Bamboo Salt

InSan Bamboo Salt (10g/day)

DIETARY_SUPPLEMENT

Placebo

Placebo (10g/day)

Sponsors & Collaborators

  • Chonbuk National University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-11-21
Primary Completion
2013-07-25
Completion
2013-07-25

Countries

  • South Korea

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01735136 on ClinicalTrials.gov