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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03891849
Other study ID # PI2018_843_0016
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date September 1, 2021
Est. completion date May 2023

Study information

Verified date February 2023
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 2023
Est. primary completion date May 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Drug:
Octreotide Injection
Patients admitted in intensive care unit after variceal hemorrhage treated with norepinephrine perfusion will received an additional octreotide perfusion during one hour.

Locations

Country Name City State
France CHU Amiens Picardie Amiens

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline of microcirculatory flow index microcirculatory flow index will be measured with sidestream dark field handheld microscope. Baseline is before octreotide perfusion. Flow characteristics of the microvasculature will be quantified using the microcirculatory flow index (MFI) according to the recommendations from the consensus on microcirculatory imaging by De Backer et al. This index will be calculated after the image will be divided into four quadrants, and the predominant type of flow (absent = 0, intermittent = 1, sluggish = 2, abnormal = 3, and hyperdynamic = 4) would be estimated in the vessels smaller than 25 µm by the operator. The final MFI score is a value obtained from the average score of the four areas. one hour after octreotide perfusion
Primary Change from baseline of microcirculatory flow index microcirculatory flow index will be measured with sidestream dark field handheld microscope. Baseline is before octreotide perfusion. Flow characteristics of the microvasculature will be quantified using the microcirculatory flow index (MFI) according to the recommendations from the consensus on microcirculatory imaging by De Backer et al. This index will be calculated after the image will be divided into four quadrants, and the predominant type of flow (absent = 0, intermittent = 1, sluggish = 2, abnormal = 3, and hyperdynamic = 4) would be estimated in the vessels smaller than 25 µm by the operator. The final MFI score is a value obtained from the average score of the four areas. 2 hours after octreotide perfusion
Primary Change from baseline of microcirculatory flow index microcirculatory flow index will be measured with sidestream dark field handheld microscope. Baseline is before octreotide perfusion. Flow characteristics of the microvasculature will be quantified using the microcirculatory flow index (MFI) according to the recommendations from the consensus on microcirculatory imaging by De Backer et al. This index will be calculated after the image will be divided into four quadrants, and the predominant type of flow (absent = 0, intermittent = 1, sluggish = 2, abnormal = 3, and hyperdynamic = 4) would be estimated in the vessels smaller than 25 µm by the operator. The final MFI score is a value obtained from the average score of the four areas. 6 hours after octreotide perfusion
Primary Change from baseline of microcirculatory flow index microcirculatory flow index will be measured with sidestream dark field handheld microscope. Baseline is before octreotide perfusion. Flow characteristics of the microvasculature will be quantified using the microcirculatory flow index (MFI) according to the recommendations from the consensus on microcirculatory imaging by De Backer et al. This index will be calculated after the image will be divided into four quadrants, and the predominant type of flow (absent = 0, intermittent = 1, sluggish = 2, abnormal = 3, and hyperdynamic = 4) would be estimated in the vessels smaller than 25 µm by the operator. The final MFI score is a value obtained from the average score of the four areas. 12 hours after octreotide perfusion
Primary Change from baseline of microcirculatory flow index microcirculatory flow index will be measured with sidestream dark field handheld microscope. Baseline is before octreotide perfusion. Flow characteristics of the microvasculature will be quantified using the microcirculatory flow index (MFI) according to the recommendations from the consensus on microcirculatory imaging by De Backer et al. This index will be calculated after the image will be divided into four quadrants, and the predominant type of flow (absent = 0, intermittent = 1, sluggish = 2, abnormal = 3, and hyperdynamic = 4) would be estimated in the vessels smaller than 25 µm by the operator. The final MFI score is a value obtained from the average score of the four areas. 24 hours after octreotide perfusion
Secondary percentage of perfused vessels percentage of perfused vessels will be measured with sidestream dark field handheld microscope before and one hour after octreotide perfusion
Secondary percentage of perfused vessels percentage of perfused vessels will be measured with sidestream dark field handheld microscope 2 hours after octreotide perfusion
Secondary percentage of perfused vessels percentage of perfused vessels will be measured with sidestream dark field handheld microscope 6 hours after octreotide perfusion
Secondary percentage of perfused vessels percentage of perfused vessels will be measured with sidestream dark field handheld microscope 12 hours after octreotide perfusion
Secondary percentage of perfused vessels percentage of perfused vessels will be measured with sidestream dark field handheld microscope 24 hours after octreotide perfusion
Secondary functional capillary density functional capillary density will be measured with sidestream dark field handheld microscope before and one hour after octreotide perfusion
Secondary functional capillary density functional capillary density will be measured with sidestream dark field handheld microscope 2 hours after octreotide perfusion
Secondary functional capillary density functional capillary density will be measured with sidestream dark field handheld microscope 6 hours after octreotide perfusion
Secondary functional capillary density functional capillary density will be measured with sidestream dark field handheld microscope 12 hours after octreotide perfusion
Secondary functional capillary density functional capillary density will be measured with sidestream dark field handheld microscope 24 hours after octreotide perfusion
Secondary Mean arterial pressure Mean arterial pressure before and one hour after octreotide perfusion
Secondary Mean arterial pressure Mean arterial pressure 2 hours after octreotide perfusion
Secondary Mean arterial pressure Mean arterial pressure 6 hours after octreotide perfusion
Secondary Mean arterial pressure Mean arterial pressure 12 hours after octreotide perfusion
Secondary Mean arterial pressure Mean arterial pressure 24 hours after octreotide perfusion
Secondary heart rate heart rate before and one hour after octreotide perfusion
Secondary heart rate heart rate 2 hours after octreotide perfusion
Secondary heart rate heart rate 6 hours after octreotide perfusion
Secondary heart rate heart rate 12 hours after octreotide perfusion
Secondary heart rate heart rate 24 hours after octreotide perfusion
Secondary ejection fraction ejection fraction before and one hour after octreotide perfusion
Secondary ejection fraction ejection fraction 2 hours after octreotide perfusion
Secondary ejection fraction ejection fraction 6 hours after octreotide perfusion
Secondary ejection fraction ejection fraction 12 hours after octreotide perfusion
Secondary ejection fraction ejection fraction 24 hours after octreotide perfusion
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