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A multicenter randomized controlled clinical study on Shenling Baizhu Powder with modifications for the treatment of eosinophilic gastritis with syndrome of spleen deficiency and dampness retention.

A multicenter randomized controlled clinical study on Shenling Baizhu Powder with modifications for the treatment of eosinophilic gastritis with syndrome of spleen deficiency and dampness retention.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000838
Enrollment
Unknown
Registered
2026-03-31
Start date
2026-04-06
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Eosinophilic Gastritis

Interventions

Experimental Group:Magnesium aluminum carbonate tablets + Shenling Baizhu powder formula with modifications
Control Group:Magnesium aluminum carbonate tablets + placebo

Sponsors

Wangjing Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Age 18-70 years, gender. 2) Confirmed diagnosis of eosinophilic gastritis through endoscopy and histopathological examination. 3) Signed informed consent, willing to participate in this study and comply with the study regulations. 4) No other severe diseases or complications, able to tolerate the treatment and follow-up of this study.

Exclusion criteria

Exclusion criteria: 1) Patients with other severe diseases, such as malignant tumors, severe cardiovascular and cerebrovascular diseases, or impaired liver and kidney function. 2) Individuals allergic to the components of Shenling Baizhu Powder or with known severe adverse reactions. 3) Pregnant or breastfeeding women. 4) Those who have recently used drugs or treatment methods that may affect the study results (e.g., glucocorticoids, immunosuppressants, etc.). 5) Individuals with a history of mental illness or unable to cooperate with the study.

Design outcomes

Primary

MeasureTime frame
Histopathological remission rate;

Secondary

MeasureTime frame
Stomach eosinophil count;Eosinophil count;Eosinophilic Gastritis Histological Scoring;Eosinophilic Gastritis Endoscopic Scoring;Patient-Reported Outcomes Measurement Information System (PROMIS) - Gastrointestinal Symptoms Scale;Severity of Dyspepsia Assessment Scale (SODA);TCM syndromology scoring system;

Countries

China

Contacts

Public ContactLiu Dengke

China Academy of Traditional Chinese Medicine Wangjing Hospital

sxxtyy@sina.com13601233816

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026