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Study to Evaluate the Effect of "Shumu Liujunzi Decoction" combined with Endoscopic Treatment on the Quality of Life and Clinical Outcomes in Patients with Type 1 Gastric Neuroendocrine Tu

Study to Evaluate the Effect of "Shumu Liujunzi Decoction" combined with Endoscopic Treatment on the Quality of Life and Clinical Outcomes in Patients with Type 1 Gastric Neuroendocrine Tu

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006581
Enrollment
Unknown
Registered
2022-09-11
Start date
2022-09-10
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

Type 1 gastric neuroendocrine tumor

Interventions

Experimental group:Shumu Liujunzi Decoction combined with Endoscopic Treatment
Controlled group:Placebo combined with Endoscopic Treatment

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1)Age = 18 years old (2)According to the WHO (5th) classification and grading standards for gastrointestinal / hepatobiliary pancreatic neuroendocrine tumors in 2019, combined with the CSCO guidelines for diagnosis and treatment of neuroendocrine tumors (2021 Edition), type 1 g-nets were diagnosed: gastric neuroendocrine tumors (netg1 or netg2) with good differentiation were pathologically diagnosed. Serum gastrin was elevated, gastric parietal cell antibodies were positive, internal factor antibodies were positive, vitamin B12 was deficient, and gastroscopy showed multiple and polypoid lesions, Gastroscopy and pathology suggested (autoimmune) atrophic gastritis, HP (-), exclusion type 2 g-nets. (3)Informed consent was signed.

Exclusion criteria

Exclusion criteria: (1)Have a history of malignant tumors of other parts and types (2)Have a history of gastric surgery (3)Taking proton pump inhibitors and H2 receptor blockers for at least 3 months (4)Combined with serious diseases that affect the evaluation of the study (5)Participated in clinical research of other drugs within 3 months before participating in the project (6)Patients in preparation for pregnancy (7)Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Recurrence rate of the Tumor;

Secondary

MeasureTime frame
Changes of pathological grade in gastroscopic biopsy;Changes of endoscopic grading of atrophic gastritis;Improvement degree of EORTCQLQ–GI.NET21 scale;Recurrence time of the Tumor;Improvement degree of QLQ-C30 scale;Improvement of TCM symptom scores;

Countries

China

Contacts

Public ContactTan Huangying
tanhuangying@263.net13811347712

Outcome results

None listed

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