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Macro and Microcirculatory Effects of the Combination of Norepinephrine and Octreotide for the Treatment of Cirrhotic Patients With Hemorrhagic Shock (HemodyNoOc)

C

Centre Hospitalier Universitaire, Amiens

Status

Withdrawn

Conditions

Variceal Hemorrhage
Haemorrhagic Shock

Treatments

Drug: Octreotide Injection

Study type

Interventional

Funder types

Other

Identifiers

NCT03891849
PI2018_843_0016

Details and patient eligibility

About

Octreotide is used to decrease portal pressure of cirrhotic patients admitted for variceal bleeding. When patients are in haemorrhagic shock, the recommended drug to increase arterial pressure is norepinephrine. Microcirculatory effects of octreotide when it is added to noradrenaline has not been investigated yet. The aim of the study is to evaluate the effect of octreotide plus norepinephrine for patient with haemorrhagic shock after variceal bleeding.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients more than 18 years old
  • patient with liver cirrhosis
  • patient with haemorrhagic shock due to variceal bleeding
  • patient with an arterial blood pressure less than 65 mmHg despite
  • patient able to express consent
  • signed written informed consent form
  • patient covered by national health insurance

Exclusion criteria

  • patient less than 18 years old
  • patient non covered by national health insurance
  • pregnant or breast feeding patent
  • known octreotide allergy
  • cardiac arrest because of shock
  • refused consent

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

octreotide (25 µg/hour) perfusion
Experimental group
Description:
octreotide (25 µg/hour) plus norepinephrine will be administered for patient with haemorrhagic shock after variceal bleeding during 2 to 5 days according recommendations and regular protocol in the medical unit
Treatment:
Drug: Octreotide Injection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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