Suspended

Endo_eAAAMeasurement of the Endothelial Function in Patients With a Abdominal Aortic Aneurism.

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What is being tested

Plasma

+ Plasma

Other
Who is being recruted

Over 18 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Diagnostic Study

Interventional
Study Start: April 2013
See protocol details

Summary

Principal SponsorRigshospitalet, Denmark
Study ContactThomas B Jørgensen, MDMore contacts
Last updated: April 17, 2013
Sourced from a government-validated database.Claim as a partner

Study start date: April 1, 2013

Actual date on which the first participant was enrolled.

50 patients is scheduled for enrollment. Blood samples will be up taken before surgery, 10 min after reperfusion, at the end of surgery and the following morning. In addition the investigators are placing a renal venous catheter where blood samples will be up taken as mentioned above for the analysis of endothelial markers together with markers for kidney damage. The first 10 patient will act as part of a pilot study, where only measurement of the endothelial and renal failure markers will be performed.

Principal SponsorRigshospitalet, Denmark
Study ContactThomas B Jørgensen, MDMore contacts
Last updated: April 17, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

50 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Diagnostic Study

Diagnostic studies focus on improving how we detect or confirm a disease. They test new tools or techniques that could provide faster or more accurate diagnoses.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

1 inclusion criteria required to participate
above 18 years

1 exclusion criteria prevent from participating
prior engagement in scientific study within the last 30 days

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Active Comparator
2 portions of FFP will be transfused prior to reperfusion

Group II

Experimental
2 portions of non-frozen plasma will be transfused prior to reperfusion

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Rigshospitalet

Copenhagen, DenmarkOpen Rigshospitalet in Google Maps
SuspendedOne Study Center