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Clinical observation of Shihu Yiwei Fang in improving gastric mucosa erosion in patients with chronic non-atrophic gastritis (Weiyin Buzu syndrome)

Clinical observation of Shihu Yiwei Fang in improving gastric mucosa erosion in patients with chronic non-atrophic gastritis (Weiyin Buzu syndrome)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006571
Enrollment
Unknown
Registered
2022-09-08
Start date
2022-08-29
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

Chronic non-atrophic gastritis with erosion

Interventions

The treatment group:Shihu Yiwei Fang
The control group:Rebamipide Tablets

Sponsors

Affiliated Hospital of Changchun University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Meeting the Western diagnostic criteria for chronic non-atrophic gastritis with erosion. (2) It meets the standard of TCM diagnosis of Weiyin Buzu syndrome. (3) Age 18-70 (including 18 and 70).

Exclusion criteria

Exclusion criteria: (1) Patients with gastric and duodenal ulcers, gastritis with active bleeding, atrophic gastritis, gastric mucosal dysplasia or suspected malignant change by pathological diagnosis. Patients with gastrointestinal bleeding or after gastric surgery. (2) Combined with cardiovascular, cerebrovascular, liver, kidney, endocrine, hematopoietic system and other serious primary diseases, as well as other diseases other than chronic non-atrophic gastritis that affect the experimental drug observation. (3) Taking proton pump inhibitors, bismuth, antibiotics and other drugs that affect the efficacy observation within one month. (4) Helicobacter pylori infection. (5) Women who are pregnant or recently preparing to become pregnant, breast-feeding women. (6) Allergic constitution or components of the drug. (7) Participate in other clinical trials within 3 months.

Design outcomes

Primary

MeasureTime frame
Improvement rate of gastric mucosal erosion under gastroscopy;

Secondary

MeasureTime frame
TCM syndrome integration;Symptoms integral;Cure rate of gastroscopic erosion of gastric mucosa;Quality of life score;Improvement rate of edema, erythema and bleeding under gastroscope;

Countries

China

Contacts

Public ContactXiongzhuang
xiongzhuang1113@sina.com13756052367

Outcome results

None listed

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