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Effect of octereotide in nonvariceal upper gastrointestinal bleeding

Randomized control trial on effect of octereotide in control of nonvariceal upper gastrointestinal bleeding

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015050322066N1
Enrollment
140
Registered
2015-11-20
Start date
2015-12-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: Upper GI bleeding. Condition 2: Upper GI bleeding. Condition 3: Upper GI bleeding. Gastric ulcer Duodenal ulcer Peptic ulcer, site unspecified

Interventions

Intervention 1: Intravenous pantoprazole 40 mg with 100 microg subcutaneous octereotide before endoscopy and pantoprazole 40 mg intravenously every 12 hours with Octreotide 100 micrograms subcutaneou
Treatment - Drugs
Placebo
Intravenous pantoprazole 40 mg with 100 microg subcutaneous octereotide before endoscopy and pantoprazole 40 mg intravenously every 12 hours with Octreotide 100 micrograms subcutaneously every 8 hour
Pantoprazole 40 mg intravenously with placebo in the same form and similar and consistent with Octreotide before endoscopy and pantoprazole 40 mg intravenously every 12 hours with subcutaneous placeb

Sponsors

Vice Chancellor of Research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: Conscious patients; age between 18 to 80 years; with complaint of melena or hematemesis or tarry stools in rectal examination Exclusion criteria: patients with congestive heart failure class 4; ESRD patients on hemodialysis; pregnant patients; Patients with acute coronary events; nursing patients; cirrhotic Patients with child score B or C; make any complications of treatment with Octreotide at any time during the study; the patient's willingness to withdraw from the study at any time during the study; taking any anticoagulant; patients suffering from coagulation diseases

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Readmission in one month after bleeding. Timepoint: one month. Method of measurement: phone calling.;Mortality in one month after bleeding. Timepoint: one month. Method of measurement: phone calling.

Secondary

MeasureTime frame
Length of hospital admission. Timepoint: daily. Method of measurement: daily visit.;Rate of blood products transfusion. Timepoint: daily. Method of measurement: visit and evaluation amounts of blood products use.;Need for surgery due to bleeding. Timepoint: hospital stay time. Method of measurement: daily visit.;Hospital readmission rate within 30 days after bleeding. Timepoint: weekly for one month. Method of measurement: weekly phone call.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoud Abrishami

Shiraz University of Medical Sciences

dr.mam55@yahoo.com+98 71 3647 4332

Outcome results

None listed

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