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An open and multi-center phase IV clinical trial of Liqinuanwei granule treatment on chronic non-atrophic gastritis

An open and multi-center phase IV clinical trial of Liqinuanwei granule treatment on chronic non-atrophic gastritis

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-15006188
Enrollment
Unknown
Registered
2015-03-24
Start date
2015-03-25
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

chronic non-atrophic gastritis

Interventions

Case series:Orally taking Liqinuanwei granule

Sponsors

Huiren Group
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnosis of chronic superficial gastritis and endoscopy or biopsy in patients diagnosed (within six months of endoscopy or pathology report issued by the hospital can be used as basis for the diagnosis, researchers archive copy; no diagnosis basis on a patient in need of endoscopy or pathology); 2. Meet TCM for disharmony and relying on cold syndrome; 3. aged 18 to 75 years old; 4. voluntary participation in clinical trials and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients combined atrophic gastritis, non-reflux esophagitis, duodenal inflammation, gastric, esophageal dysplasia or histological diagnosis of suspected malignant; 2. Patients suffered nausea and vomiting can not be excluded by acute gastroenteritis; 3. Patients suffered other severe disease, diabetes poorly controled (fasting plasma glucose >=7.0mmol/L or postprandial glucose >=11.1mmol/L), and the disease impact of living, such as cancer or AIDS; 4. Patients suffered abnormal liver function (ALT or AST more than 2 folds the upper limit of normal), renal dysfunction (Scr exceed the upper limit of normal); 5. Patients with allergies, such as two or more (including two kinds) drug or food allergies; known to be allergic to the ingredients of the drug; 6. The investigator estimate the patients with low possibility of enrollment or complicate that, such as frequent changes in the work place lead to lost easily to follow; 7. Prepared pregnancy or pregnant women (except to terminate the pregnancy), lactating women; 8. Patients with drug or alcohol dependence; 9. The patient is participating in other clinical trials; 10. Researchers do believe patients unfit to participate in clinical trials.

Design outcomes

Primary

MeasureTime frame
The main symptom scores;Pain VAS score;main symptoms disappear time;Main symptoms disappear rate;

Countries

China

Contacts

Public ContactMEI Linghua
ncmlh@163.com+86 021-50272969

Outcome results

None listed

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