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Clinical effect of Beiling Weitong Granule combined with endoscopic mucosal dissection in the treatment of undifferentiated early gastric cancer

Analysis of Clinical Efficacy and Prognosis of Endoscopic Mucosal Resection for the Treatment of Early Gastric Cancer and Precancerous Lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000548
Enrollment
Unknown
Registered
2026-03-18
Start date
2023-04-29
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Undifferentiated early gastric cancer

Interventions

Control Group:Undergo ESD procedure + oral placebo
Experimental Group:Undergo ESD procedure and take oral administration of Biling Weitong granules.

Sponsors

Xinxiang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for undifferentiated early gastric cancer as specified in the "Gastric Cancer Diagnosis and Treatment Guidelines (2018 Edition)." 2. Meets the diagnostic criteria for the Qi stagnation and blood stasis syndrome as specified in the "Chinese Medical Diagnosis and Treatment Guidelines for Malignant Tumors" (main symptoms: stabbing pain in the gastric region, discomfort below the heart; secondary symptoms: nausea, vomiting of blood, black stools, dark complexion, tongue with ecchymosis, and a deep, fine, and thready pulse). 3. Age between 18-75 years, gender. 4. Able to tolerate ESD surgery and agrees to receive treatment with Bilinguotong granules. 5. Voluntarily participates in this study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Subjects with immune dysfunction or hemostatic disorders. 2. Subjects with other primary malignant tumors. 3. Subjects with severe mental or psychological disorders who are unable to comply with treatment and follow-up. 4. Subjects with allergic constitution or known allergy to components of the investigational drug. 5. Subjects who have received other anti-tumor treatments prior to enrollment or are currently participating in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Overall clinical efficacy rate;

Secondary

MeasureTime frame
Postoperative complications;Gastrointestinal Function Recovery Indices;Pain score;Traditional Chinese Medicine Syndromes Total Score;Tumor Markers;Inflammatory Factors;

Countries

China

Contacts

Public ContactChen Yafei

Xinxiang Central Hospital

chenyaf9919@126.com18737399919

Outcome results

None listed

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