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Investigator Initiated Trial to Evaluate the Efficacy of FEXUCLUE®40mg(Fexuprazan hydrochloride) in Patients with Iatrogenic Gastric Ulcer After Endoscopic Submucosal Dissection

A Multi-center, Investigator Initiated Trial to Evaluate the Efficacy of FEXUCLUE®40mg(Fexuprazan hydrochloride) in Patients with Iatrogenic Gastric Ulcer After Endoscopic Submucosal Dissection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008892
Enrollment
105
Registered
2023-10-27
Start date
2024-07-30
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

None listed

Interventions

Drug : The control group Nexium®40 mg was set to 40 mg once a day for general artificial ulcer treatment.Fexuclujeong®40mg, a clinical trial drug, was 40mg once a day in ERD, and the dose of this clin

Sponsors

Presbyterian Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Those who receive ESD due to gastric cancer or hypothyroidism confined to the mucous membrane

Exclusion criteria

Exclusion criteria: ? A person who is sensitive to the components of a clinical trial drug ? In the case of drugs that may affect the effectiveness of gastric acid secretion inhibitors as follows, those who took them within two weeks before endoscopic mucosal surgery - - PPI, H2 receptor antagonists, mucosal protective anti-ulcer drugs ? Patients who are required to take combination of clinical trial drug licenses during the clinical trial period as follows - Combination inhibitors (atazanavir, nelpinavir, or lilphibirin-containing preparations, etc.) - Drugs that increase the risk of bleeding (such as aspirin, anti-coagulants, etc.) - - Steroid, NSAID ? I've had surgery that can affect gastric acid secretion Let's. ? Those who are unable to undergo upper gastrointestinal endoscopy (e.g., esophageal disease, gastrointestinal bleeding, etc ? Endoscopic submucosal resection is prohibited (platelet reduction, coagulation disorder, etc.) ? People with clinically significant liver and kidney disease ? A person with a history of malignant tumors within three years (However, in the case of malignant tumors except for malignant tumors of the digestive system, those who have been cured and have passed more than 3 years without recurrence from the date of judgment can register.) ? Person with bipolar disorder, anxiety disorder, panic disorder, physical form disorder, personality disorder, or other clinically significant psychiatric disorder ? a person who is pregnant or lactating

Design outcomes

Primary

MeasureTime frame
Percentage of patients with endoscopic artificial ulcers turned into scars

Secondary

MeasureTime frame
Rate of delayed bleeding

Countries

Korea, Republic of

Contacts

Public ContactJin Woong cho

Presbyterian Medical Center

jeja-1004@daum.net+82-63-230-8114

Outcome results

None listed

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