Cannulation of the Artery Axiliaris for Extracorporeal Circulation

NCT ID: NCT01615172

Last Updated: 2014-08-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-01-31

Study Completion Date

2014-12-31

Brief Summary

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Comparision of two different cannulation techniques on the neurological outcome in cardiac surcical procedures. Study hypothesis: Cannulation of the axilaris artery can reduce neurolocical side effects.

Detailed Description

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Conditions

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Neurologic Manifestations

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Aortic cannulation

routine placement of aortic cannula

Group Type ACTIVE_COMPARATOR

cannulation

Intervention Type PROCEDURE

The different types of cannulation (aortic versus axillaris) were compared in the postoperative period for neurological deficits in three time periods.(intraoperative, 5.POD, 3 month POD)

axilaris cannulation

new type of cannulation

Group Type ACTIVE_COMPARATOR

cannulation

Intervention Type PROCEDURE

The different types of cannulation (aortic versus axillaris) were compared in the postoperative period for neurological deficits in three time periods.(intraoperative, 5.POD, 3 month POD)

Interventions

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cannulation

The different types of cannulation (aortic versus axillaris) were compared in the postoperative period for neurological deficits in three time periods.(intraoperative, 5.POD, 3 month POD)

Intervention Type PROCEDURE

Other Intervention Names

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MAQUET 20, 22 and 24 Fr

Eligibility Criteria

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Inclusion Criteria

* Cardiac procedure with ecc Age 40-85 years CABG and/or valve

Exclusion Criteria

* Stenosis of a.subclavia
Minimum Eligible Age

40 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pitzer Stiftung

UNKNOWN

Sponsor Role collaborator

Johann Wolfgang Goethe University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Arndt-H. Kiessling

Cardia vascular research

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Andreas Zierer, PD.Dr

Role: PRINCIPAL_INVESTIGATOR

Goethe University

Locations

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Goethe Universität

Frankfurt am Main, Hesse, Germany

Site Status RECRUITING

Countries

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Germany

Facility Contacts

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Andreas Zierer, MD

Role: primary

+49696301 ext. 0

Other Identifiers

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AXI-001

Identifier Type: -

Identifier Source: org_study_id

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