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Study the Effect of Probiotics Combined With Bismuth Quadruple Rescue Therapy on H Pylori Infective Patients

N

Naval Military Medical University

Status

Unknown

Conditions

Helicobacter Pylori Infection

Study type

Observational

Funder types

Other

Identifiers

NCT03297242
chbs230023

Details and patient eligibility

About

Retrospectivly follow-up the outpatients for H pylori eradication failures more than 2 times in the digestive department of Changhai hospital from 2015-2017,analyse the eradication rates and adverse effects of the therapy with 2w's compound lactobacillus acidophilus followed by 10d's bismuth, furazolidone, tetracycline contained quadruple scheme.

Full description

H pylori infection rate has been up to half of the world population. H pylori infection is associated with various diseases, especially gastric cancer.

With the increasingly resistant to antibiotics,the eradication rate has decreased a lot with traditional triple therapy. Exploring a valid scheem for patients who have failed multiple times is important.

Probiotics can improve gastrointestinal microenvironment, then release the adverse effects during the eradication process.Additionally,there is also a lot evidence that probiotics can inhibit H plori,but still controversially.

There is a low resistant rate about furazolidone and tetracycline. In this study investigators observe the efficacy of the therapy 2w's compound lactobacillus acidophilus followed by 10d's bismuth, furazolidone, tetracycline contained quadruple scheme on patients who have failed more than 2 times. 4 to 6 weeks after the therapy, if Urea Breath Test (UBT) is nedative which means eradicating H plori successfully.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • H pylori eradication had failed more than 2 times
  • Patients had never used furazolone and tetracycline
  • The age varied from 18 to 80 years old

Exclusion criteria

  • H pylori initial eradication or had failed only 1 time
  • The age was lower than 18,or higher than 80 years old
  • Patients who had serious heart pulmonary disease ,live renal disease, or any cancers
  • Pregnant women

Trial contacts and locations

0

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Central trial contact

Yi Q Du, MD; Ai R Liu, MM

Data sourced from clinicaltrials.gov

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