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To elucidate the phenotypic differences and mechanism of TCM dampness and toxin deficiency intervention in gastric precancerous lesions based on the interaction of miRNAs

To elucidate the phenotypic differences and mechanism of TCM dampness and toxin deficiency intervention in gastric precancerous lesions based on the interaction of miRNAs

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000207
Enrollment
Unknown
Registered
2024-08-10
Start date
2021-04-02
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

gastric precanerous

Interventions

Pingwei Jianzhong Huashi Jiedu treatment group:Pingwei Jianzhong Jiedu prescription was given orally
usual care group:symptomatic treatment

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: Diagnostic criteria: precancerous lesions of gastric mucosa were defined as chronic atrophic gastritis with intestinal metaplasia or dysplasia according to the 2017 Chinese Medical Association Consensus on Chronic Gastritis (Shanghai), combined with endoscopic and pathological diagnosis, and the final diagnosis was based on pathological diagnosis. 1) Patients who met the above diagnostic criteria were informed and agreed to receive treatment; 2) The age of patients ranged from 35 to 65 years old.

Exclusion criteria

Exclusion criteria: Diagnostic criteria: precancerous lesions of gastric mucosa were defined as chronic atrophic gastritis with intestinal metaplasia or dysplasia according to the 2017 Chinese Medical Association Consensus on Chronic Gastritis (Shanghai), combined with endoscopic and pathological diagnosis, and the final diagnosis was based on pathological diagnosis. 1) Gastric cancer; 2) patients with other serious digestive system diseases, such as peptic ulcer, gastric bleeding, biliary tract, pancreas and other organic lesions; 3) combined with malignant tumors; 4) Complicated with serious heart, lung, liver, kidney and other system diseases; 5) who are participating or participated in other clinical trials less than 3 months after completion; 6) pregnant or lactating women; 7) with severe cognitive impairment; 8) The investigator thought that there were other conditions that were not suitable for the study.

Design outcomes

Primary

MeasureTime frame
therapeutic evaluation;

Countries

China

Contacts

Public ContactXiaobo Yang

The Second Affiliated Hospital of Guangzhou University of Chinese Medicine

yangxiaobo39358517@hotmail.com13825012636

Outcome results

None listed

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