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Comprehensive clinical evaluation of proton-pump inhibitors purchased in quantities for the treatment of acute upper gastrointestinal bleeding

Comprehensive clinical evaluation of proton-pump inhibitors purchased in quantities for the treatment of acute upper gastrointestinal bleeding

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087647
Enrollment
Unknown
Registered
2024-07-31
Start date
2023-05-01
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

Acute upper gastrointestinal bleeding

Interventions

Experimental group:High-dose intravenous esomeprazole (centralized procurement)(8 mg/hour, 192 mg/day) was given with continuous instillation for = 2 days
Control Group:High-dose intravenous esomeprazole (Original drug) (8 mg/h, 192 mg/day) continued instillation for =2 days

Sponsors

Shenzhen People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age 18 to 75; (2) Admission diagnosed with acute upper gastrointestinal bleeding (ICD-9); (3) After admission, receive high-dose intravenous PPI (8 mg/h, 192 mg/day) continuous instillation treatment, and the medication time is = 2 days.

Exclusion criteria

Exclusion criteria: (1) Patients with liver cancer; (2) Patients with severe immune system disorders who have recently taken glucocorticoids.

Design outcomes

Primary

MeasureTime frame
Further bleeding;Adverse reactions;high-dose PPI cost;

Secondary

MeasureTime frame
Death during hospitalization;Length of hospital stay;Secondary endoscopic treatment;Rehospitalization for bleeding within 30 days;

Countries

China

Contacts

Public ContactXie Shou Xia

Shenzhen People's Hospital

szshouxia@163.com+86 180 2538 8921

Outcome results

None listed

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