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Search / Trial NCT02633930

Helicobacter Pylori Eradication With Berberine Quadruple Therapy Versus Clarithromycin Quadruple Therapy

Launched by XIJING HOSPITAL OF DIGESTIVE DISEASES · Dec 16, 2015

Trial Information

Current as of September 02, 2025

Completed

Keywords

Helicobacter Pylori Berberine Containing Quadruple Therapy Clarithromycin Containing Quadruple Therapy

ClinConnect Summary

The study will include three phases: screening, treatment and follow-up. Screening: this phase will last a maximum of 28 days and subjects eligibility will be evaluated after informed consent signature. Endoscopy and Urea Breath test will be performed in addition to the baseline routine evaluations.

Treatment: Subjects are randomly assigned to treatment and will be treated for 14 days. A randomization visit will take place on Day 0 and an end-of-treatment visit will take place between day 12 and 14.

Follow-up: includes two visits. approximately 14 days of treatment and 28 days after the e...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Age between 18\~70,both gender.
  • 2. Patients with upper gastrointestinal symptoms and with documented H.pylori infection.
  • 3. Patients are willing to receive eradication treatment.
  • 4. Women are eligible if they are not pregnant or nursing, and if they are of childbearing potential they are required to use medically acceptable contraception for the duration of the study and 30 days thereafter.
  • Exclusion Criteria:
  • 1. Patients are excluded if they have previously used antibiotics to eradicate adequately recorded infection with H. pylori.
  • 2. Contraindications to study drugs.
  • 3. Substantial organ impairment, severe or unstable cardiopulmonary or endocrine disease.
  • 4. Constant use of anti-ulcer drugs ( including taking proton-pump. inhibitors(PPI) within 2 weeks before the \[13C\] urea breath test), antibiotics or bismuth complexes (more than 3 times /1 month before screening)
  • 5. Pregnant or lactating women.
  • 6. Underwent upper gastrointestinal Surgery.
  • 7. Patients with Barrett esophageal or highly atypical hyperplasia, have symptom of dysphagia.
  • 8. Evidence of bleeding or iron efficiency anemia.
  • 9. A history of malignancy.
  • 10. Drug or alcohol abuse history in the past 1 year.
  • 11. Systemic use of corticosteroids, non steroidal anti-inflammatory drugs, anticoagulants, platelet aggregation inhibitors (except the use of aspirin for less than 100 mg/d).
  • 12. Enrolled in other clinical trials in the past 3 months.

About Xijing Hospital Of Digestive Diseases

Xijing Hospital of Digestive Diseases is a leading medical institution specializing in the diagnosis and treatment of gastrointestinal disorders. Affiliated with the Fourth Military Medical University in Xi'an, China, the hospital is renowned for its cutting-edge research and commitment to advancing digestive health. With a multidisciplinary team of experts, Xijing Hospital conducts innovative clinical trials aimed at improving patient outcomes and enhancing therapeutic strategies in digestive diseases. The institution is dedicated to fostering collaboration and excellence in clinical research, contributing significantly to the global understanding of gastrointestinal health and disease management.

Locations

Xi'an, Shanxi, China

Xi'an, Shanxi, China

Patients applied

0 patients applied

Trial Officials

Yongquan Shi, Ph. D

Principal Investigator

Xijing Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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