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Study on effect of Helicobacter pylori eradication therapy on ulcer healing after endoscopic submucosal dissection for gastric tumor

Study on effect of Helicobacter pylori eradication therapy on ulcer healing after endoscopic submucosal dissection for gastric tumor - Study on effect of Helicobacter pylori eradication therapy on ulcer healing after endoscopic submucosal dissection for gastric tumor

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010772
Enrollment
500
Registered
2013-05-24
Start date
2013-05-24
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

H. pylori-positive gastric tumor (early gastric cancer or gastric adenoma)

Interventions

After ESD, 20 mg of omeprazole will be intravenously administered twice a day for 2 days. After that, esomeprazole 20 mg, amoxicillin 750 mg, and clarithromycin 400 mg will be orally administered twic

Sponsors

Research Organization for Gastroenterological Disease Treatment
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) early gastric cancer (absolute indication for ESD in the Gastric Cancer Treatment Guidelines) or gastric adenoma (=< 20 mm) (2) a single gastric tumor (3) no histry of medication or radiotherapy for other cancer within past 3 years (4) H. pylori positive (5) twenty years or older (6) voluntary written informed consent to participate in the study

Exclusion criteria

Exclusion criteria: (1) history of H. pylori eradication therapy (2) concurrent gastric or duodenal ulcer, except for ulcer scarring (3) history of upper gastrointestinal tract resection or vagotomy (4) gastrointestinal tract warning symptoms (5) serious hepatic disease (6) serious renal disease (7) currently receiving antithrombotic therapy (8) contraindication or hypersensitivity to the study drugs (9) pregnant, possibly pregnant and lactating woman (10) determined as inappropriate to participate in the study by the investigator

Design outcomes

Primary

MeasureTime frame
The ulcer scarring rate at 8 weeks (56 days) after the start of allocation treatment.

Countries

Japan

Contacts

Public ContactToshihisa Takeuchi

Osaka Medical College Endoscopic Center

in2097@poh.osaka-med.ac.jp072-683-1221

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026