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Clinical studies on the efficacy of eradicating Helicobacter pylori by Saccharomyces boulardii in combination with standard triple therapy

Clinical studies on the efficacy of eradicating Helicobacter pylori by Saccharomyces boulardii in combination with standard triple therapy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003348
Enrollment
Unknown
Registered
2013-05-26
Start date
2013-06-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

diseases of upper gastrointestinal

Interventions

Group A:Taking standard triple drug
Group B:Taking Saccharomyces boulardii scattered and standard triple drug

Sponsors

Daping Hospital, the Third Military Medical University, Chongqing, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. chronic gastritisor or duodenal ulcer patients without complicated; 2. rapid urease test was positive (>=2+) or 13C-breath test was positive before and after a week undergo endoscopy; 3. aged from 18 to 60,both male and female; 4. not received formal Hp eradication therapy before; 5. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. used antibiotics, bismuth, probiotics, H2 receptor antagonists and PPI 2 weeks before treatment; 2. pregnant or lactating women; 3. taking non-steroidal anti-inflammatory drugs or alcohol,or severe liver disease, heart disease, kidney disease, cancer and other diseases; 4. drug allergy patients; 5. gastrectomy patients; 6. 3 months prior to participating in other drug studies; 7. difficult to follow-up or to complete the various factors affecting.

Design outcomes

Primary

MeasureTime frame
Hp eradication rate;

Secondary

MeasureTime frame
Incidence of adverse reaction;

Countries

China

Contacts

Public ContactLan ChunHui
tiandaochouqin99@hotmail.com+86 13896067955

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026