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Role of Statin on the Gastric Inflammation in Patients at High Risk of Gastric Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01813994
Enrollment
96
Registered
2013-03-19
Start date
2014-11-30
Completion date
2018-06-19
Last updated
2019-03-29

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

Conditions

Early Gastric Cancer or Gastric Adenoma

Keywords

Statin; Gastric inflammation; Gastric cancer

Brief summary

Statins are commonly used as cholesterol-lowering medications and have shown effectiveness in the primary and secondary prevention of heart attack and stroke. In addition, several recent studies of human cancer cell lines and animal tumor models indicate that statins may have chemopreventive properties through the arresting of cell-cycle progression. The chemopreventive effect of statins was demonstrated in some kind of human tumors including colorectal cancer. In addition, recent one large epidemiologic study showed that statins decreased risk of gastric cancer. On the other hands, it has been well known that Helicobacter pylori infection induces gastric atrophy and intestinal metaplasia, which are premalignant lesions of gastric cancer. Progression of these premalignant lesions could be limited by H. pylori eradication. In addition, a recent double blind randomization study revealed that simvastatin as adjuvant to standard therapy improves significantly the H. pylori eradication rate. Therefore, investigators conjecture that statins may have an adjuvant role for inhibition of gastric carcinogenesis. investigators aim to evaluate the role of statins in gastric carcinogenesis by observing the changes of gastric inflammation under statins.

Interventions

DRUGArm1: Statin

Study1 (only H. pylori infected patients) Arm1: All patients undergo H. pylori eradication therapy after 2 weeks from the endoscopic submucosal dissection. In this arm2, all patients take statins for 6 months. Then, follow-up endoscopy for gastric biopsy and CLO test will be performed after 6.5 months from the endoscopic submucosal dissection. Study2 (only H. pylori non-infected patients) Arm1: In this arm2, all patients start taking statins after 2 weeks from the endoscopic submucosal dissection. Follow-up endoscopy for gastric biopsy will be performed after 6.5 months from the endoscopic submucosal dissection.

DRUGArm2: Placebo

Study1 (only H. pylori infected patients) Arm2: All patients undergo H. pylori eradication therapy after 2 weeks from the endoscopic submucosal dissection. In this arm2, all patients take placebos for 6 months. Then, follow-up endoscopy for gastric biopsy and CLO test will be performed after 6.5 months from the endoscopic submucosal dissection. Study2 (only H. pylori non-infected patients) Arm2: In this arm2, all patients start taking placebos after 2 weeks from the endoscopic submucosal dissection. Follow-up endoscopy for gastric biopsy will be performed after 6.5 months from the endoscopic submucosal dissection.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Age, between 20 and 70 2. Early gastric cancer or adenoma which is achieved curative resection by endoscopic submucosal dissection 3. ECOG performance status 0 or 1

Exclusion criteria

1. Previous subtotal gastrectomy or gastrostomy 2. Repeated endoscopic submucosal dissection 3. Two or more synchronous lesions 4. Presence of gastric or duodenal ulcer except artificial ulcer due to endoscopic submucosal dissection 5. History of drugs which are able to induce gastric ulcer including aspirin, NSAIDs, and steroid (30 days or more, within 1 year at the time of screening 6. Indication of statins, including dyslipidemia, myocardial infarction, and heart failure. 7. Develop of complications caused by endoscopic submucosal dissection, including bleeding, perforation, and pneumonia 8. LDL \< 70 mg/dL 9. Allergy to statins 10. Pregnancy or breast milk feeding 11. Active infection 12. Significant cardiopulmonary disease 13. Active hepatitis or severe hepatic dysfunction 14. Severe renal dysfunction 15. Severe bone marrow dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Proportion of the patients with high-risk (III/IV) OLGA stages6 months from the start of taking the statinspatients with high-risk OLGA stages will be assessed by histologic examinations

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026