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The effects and security of JianWei Qutong pill on the treatment of chronic non-atrophic gastritis (spleen and stomach Qi deficiency with damp-heat stasis syndrome): randomized, double-blind, placebo-controlled, multi-center Phase ? clinical trial study

The effects and security of JianWei Qutong pill on the treatment of chronic non-atrophic gastritis (spleen and stomach Qi deficiency with damp-heat stasis syndrome): randomized, double-blind, placebo-controlled, multi-center Phase ? clinical trial study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004088
Enrollment
Unknown
Registered
2014-01-03
Start date
2014-02-03
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

Group 1:placebo-controlled
Group 2:low dose
Group 3:High dose

Sponsors

Department of Integrated Traditional Chinese and Western Medicine, West China Hospital, West China School of Medicine, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Fulfilling the Western Medicine diagnosis of chronic non-atrophic gastritis (chronic inflammation is moderate and above, and / or active inflammation); 2. Fulfilling the TCM diagnosis of spleen and stomach Qi deficiency with damp-heat stasis syndrome; 3. Aged between 18-65 years old; 4. Willing to participate and sign the inform consent.

Exclusion criteria

Exclusion criteria: 1. history of gastric surgery; 2. Combined stomach?duodenum ulcer, special type of gastritis, peptic ulcer, bleeding, gastric mucosa dysplasia or suspected malignant pathologically; 3. pathological examinations showed atrophy and / or intestinal metaplasia lesions; 4. combined cardiovascular, lung, liver, kidney and hematopoietic systems severe primary disease (above NYHA II; ALT, AST 1.5 times of the upper limit of normal; Cr over the upper limit of normal), or diseases which severely affect their survival, such as cancer or AIDS; 5. fecal occult blood is positive; 6. had received other TCM treatment to treat this disease in the last two weeks; 7. mental illness or alcohol / drug abuse history; 8. pregnancy or prepare pregnant women, lactating women; 9. allergies or allergic to the known ingredient of the test drug; 10. participated or are participating in clinical trials by other drugs within the past three months; 11. syndrome differentiation is not clear or there are too many combinations and syndromes; 12. Researchers who consider it's not appropriate to participate in clinical trials.

Design outcomes

Primary

MeasureTime frame
epigastric pain disappearance rate;

Secondary

MeasureTime frame
Visual analogue scale method (VAS) changes before and after treatment;primary treatment effect;

Countries

China

Contacts

Public ContactXia Qing

West China Hospital, West China School of Medicine, Sichuan University

xiaqing@medmail.com.cn+86 18980601723

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026