Preoperative Microcirculation and Postoperative Outcome After Major Vascular Surgery

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

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2021-02-01

Study Completion Date

2022-02-01

Brief Summary

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The aim of the study is to determine whether there is a correlation between the microcirculation measured preoperatively in patients undergoing major vascular surgery and the postoperative mortality during hospitalization period. The microcirculation will be measured sublingually with the Cytocam-IDF imaging technique.

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Detailed Description

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Conditions

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Surgery--Complications

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Patients will be split into two groups after data collection. They will receive the same treatment during the clinical trial.

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Cytocam-IDF Imaging

All patients will undergo the same interventional test.

Group Type OTHER

Cytocam-IDF imaging device

Intervention Type OTHER

Observation of the microcirculation

Interventions

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Cytocam-IDF imaging device

Observation of the microcirculation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age ≥ 18 years

* Males and females
* ASA III classification
* Written informed consent obtained by the patient
* Elective hospital admission for major vascular surgery, both open and endovascular

Exclusion Criteria

* Emergency surgery

* Minor vascular procedures (e.g. varicose vein stripping; thromboembolectomy; vascular access formation)
* Pregnancy
* Refusal or inability to provide written informed consent (language barrier, mental retardation)

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No