Efficacy and Safety of Hizikia Fusiformis Extract in Subjects Showing Erosive Gastritis

C

Chonbuk National University

Status

Completed

Conditions

Erosive Gastritis

Treatments

Dietary Supplement: Placebo
Dietary Supplement: Hizikia Fusiformis extract

Study type

Interventional

Funder types

Other

Identifiers

NCT01689701
PKU-EG-ECKL

Details and patient eligibility

About

The investigators performed a double-blind parallel study in a group of Subjects Showing Erosive Gastritis who were given Hizikia Fusiformis Extract over a period of 4 weeks. Endoscopic observations were performed before and 4 weeks after the treatment, and the cure and improvement rates were investigated.

Enrollment

54 patients

Sex

All

Ages

19 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Males and females 19-70 years old
  • Subjects Showing Erosive Gastritis (endoscopy)
  • Able to give informed consent

Exclusion criteria

  • Diagnosed of gastrointestinal disease such as ulcer, cancer within 1 months
  • Allergic or hypersensitive to any of the ingredients in the test products
  • History of disease that could interfere with the test products or impede their absorption, such as gastrointestinal disease or gastrointestinal surgery
  • Taken antibiotics and stomach medicines such as steroid, bismuth compound and proton pump inhibitor within 1 months
  • Participation in any other clinical trials within past 2 months
  • Laboratory test, medical or psychological conditions deemed by the investigators to interfere with successful participation in the study
  • Pregnant or lactating women etc.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

54 participants in 2 patient groups, including a placebo group

Hizikia Fusiformis extract
Experimental group
Treatment:
Dietary Supplement: Hizikia Fusiformis extract
Placebo
Placebo Comparator group
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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