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Clinical evaluation of Jinghua Weikang Capsule in the treatment of Helicobacter pylori infection in the elderly: a randomized, placebo-conrtolled trial

Clinical evaluation of Jinghua Weikang Capsule in the treatment of Helicobacter pylori infection in the elderly

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR1900002852
Enrollment
Unknown
Registered
2019-12-20
Start date
2020-01-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Health development and scientific reasearch in the capital

Interventions

Group1:Taking Jinghuaweikang capsule analog for 28 days
Group2:Taking Jinghuaweikang capsule for 28 days

Sponsors

Peking Univeisity First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 65 years, genders are unlimited; 2. HP infection was diagnosed by urea 13C breath test, endoscopic rapid urease test or stool antigen test; 3. Except for gastrointestinal tumor and other space occupying lesions through endoscope or abdominal CT, gastrointestinal ultrasound, gastrointestinal contrast radiography and other imaging test; 4. There are more than two chronic diseases such as diabetes, dyslipidemia, cardiovascular and cerebrovascular diseases, hypertension, thyroid dysfunction, COPD, immune system diseases, or two or more drugs taken orally for a long time ( >= 3 months); 5. No antibiotics within 1 month, no acid inhibitors or or bismuth agent within 2 weeks; 6. The subjects (or legal representatives) voluntarily consented and signed informed consent and were able to follow the research program during the study.

Exclusion criteria

Exclusion criteria: 1. Having a history of gastric surgery; 2. Having active gastrointestinal bleeding and peptic ulcer; 3. With serious diseases affecting the evaluation of the study, such as serious liver disease, heart disease, kidney disease, malignant tumor and alcoholism; 4. Allergic to the drugs applied in the study; 5. With low lung function; 6. Having participated in other drug clinical studies within 3 months before participating in this project; 7. Patients could not express their subjective feelings correctly and could not cooperate with each other.

Design outcomes

Primary

MeasureTime frame
Score of symptoms;Breath;

Countries

China

Contacts

Public ContactHui Ye
brightleaf723@163.com+86 010 83572351

Outcome results

None listed

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