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Noninferiority of Ilaprazole Sodium for Injection in the prevention and treatment of inpatients with nonvaricose upper gastrointestinal bleeding: a real-world, multicenter, retrospective, observational study

Noninferiority of Ilaprazole Sodium for Injection in the prevention and treatment of inpatients with nonvaricose upper gastrointestinal bleeding: a real-world, multicenter, retrospective, observational study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073453
Enrollment
Unknown
Registered
2023-07-11
Start date
2021-05-01
Completion date
Unknown
Last updated
2023-07-16

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

Conditions

Nonvaricose upper gastrointestinal bleeding

Interventions

Sponsors

Guangdong Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Hospitalized cases; (2) There is no limitation on gender or age; (3) Use of Ilaprazole Sodium for Injection or Esomeprazole Sodium for Injection for more than 2 days (=3 days).

Exclusion criteria

Exclusion criteria: (1) Hospitalized patients who used other PPI or H2 receptor antagonists (omeprazole, Lansoprazole, pantoprazole, rabeprazole, cimetidine, ranitidine, Famotidine, nizatidine, Roxatidine, ebromotidine, and miphentidine) in combination; (2) Patients who used Ilaprazole Sodium for Injection and Esomeprazole Sodium for Injection; (3) Deaths not caused by gastrointestinal bleeding; (4) Clinically confirmed cases of upper digestive tract tumor; (5) Clinically confirmed cases of varicose upper gastrointestinal bleeding; (6) Clinically confirmed cases of lower gastrointestinal bleeding.

Design outcomes

Primary

MeasureTime frame
Prevention success rate;Hemostatic effective rate;Adverse reaction;

Countries

China

Contacts

Public ContactWeihua Lai

Guangdong Provincial People's Hospital

pde@gdyl.org+86 138 2449 2310

Outcome results

None listed

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