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Clinical Trials/IRCT201202289160N1
IRCT201202289160N1CompletedPhase 3

Comparison the therapeutic effects of high-dose and low-dose pantoprazole after endoscopy in patients with peptic ulcer bleeding

Research Deputy of Ahvaz University of Medical Sciences0 sites166 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor
Enrollment
166

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
16 years to 70 years (—)
Sex
All

Inclusion Criteria

  • patients who admit and present signs and symptoms of upper gastrointestinal bleeding such as: 1-Vomits of blood or black material (Hematemesis), 2-Black and tarry stool (Melena), 3-The passage of bright red or blood from the rectum (Hematochesia), 4-Vertigo; light headness and hypotension. Exclusion criteria are: 1-Malignant ulcer; 2-Multiple ulcers; 3-Cirrhotic patient with coagulopathy or hemorrhagic varices; 4-Chronic Renal Failure (CRF); 5-Patients who admitted with gastrointestinal bleeding in last month; 6-Patients receive NSAID and Corticosteroid for underlying disease; 7-Patients under 16 years or upper 70 years;8-Patients who are treated with PPI (proton pomp inhibitor) in last week.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Research Deputy of Ahvaz University of Medical Sciences

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