Skip to content

Prospective observational cohort study on the efficacy and safety of Evodia Radix Recipe in the treatment of chronic non-atrophic gastritis

Compatibility evaluation and biological basis of Evodia Fructus Recipe based on combination of clinical disease and syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2200006408
Enrollment
Unknown
Registered
2022-08-01
Start date
2022-08-01
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

Chronic non-atrophic gastritis

Interventions

Stomach heat syndrome:Zuojin pill
Stomach cold syndrome:Wuzhuyu decoction

Sponsors

Fifth Medical Center of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? Age 18 to 65 years old, male or female; ? Western medicine diagnosed as chronic non-atrophic gastritis; ? TCM syndrome differentiation is the liver-fire invading stomach syndrome or liver-stomach deficiency-cold syndrome; ? Subjects of childbearing age who voluntarily take effective contraceptive measures during the trial; ? Voluntarily signed the informed consent.

Exclusion criteria

Exclusion criteria: ? Gastroscopy with esophageal disease, peptic ulcer, tumor, bleeding lesions; ? Combined with severe dysplasia of gastric mucosa and pathological diagnosis of suspected malignant transformation; ? Patients with autoimmune gastritis were excluded by serum gastrin, vitamin B12 levels and related autoantibodies (anti-parietal cell antibodies and anti-intrinsic factor antibodies); ? Have serious primary heart, liver, lung, kidney, blood or serious diseases that affect their survival, such as tumors, AIDS or coagulation disorders; ? Laboratory examination: Scr>N (N is the upper limit of normal value); ALT, AST>N; white blood cells <3.0×109/L; ? Allergic constitution, such as those who are allergic to drugs or food; or those who are known to be allergic to research drugs; ? Patients with alcoholism and drug dependence, with a history of epilepsy or with mental disorders; ? Pregnant, lactating women or those planning to become pregnant; ? Those who have participated in or are participating in other clinical trials within 3 months; ? Other patients deemed unsuitable for the study by the investigator.

Design outcomes

Primary

MeasureTime frame
Clinical observational indicators;Liver damage indicators;Kidney damage indicators;Nerve damage evaluation index;

Secondary

MeasureTime frame
Histopathological findings;TCM syndrome score;Endogenous metabolites;Clinical efficacy indicators;Gastroscopy results;

Countries

China

Contacts

Public ContactYanling Zhao

Chinese People's Liberation Army General Hospital

zhaoyl2855@126.com13681208998

Outcome results

None listed

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