The Influence of Preoperative Cardiopulmonary Capacity on the Perioperative Lactate Level

NCT ID: NCT01819337

Last Updated: 2013-09-17

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

COMPLETED

Total Enrollment

1502 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-03-31

Study Completion Date

2013-08-31

Brief Summary

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The aim of this study is to identify if there exists a correlation between the preoperative cardiopulmonary capacity - measured in MET's - and the perioperative lactate serum level.

Detailed Description

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The determination of the cardiopulmonary (c/p) capacity is very important for the evaluation of every patient undergoing surgery. The ability to climb at least two flight of stairs is seen to be an acceptable c/p capacity for surgery. There are several ways to evaluate the fitness of patients. A common method to estimate the cardiopulmonary capacity is defining patients through the MET's (metabolic equivalents) scale. MET's can be defined relatively easy through a simple questionnaire. Patients with a reduced c/p capacity have less than 4 MET's, patients with a relatively good c/p capacity have 4-10 MET's and patients with a excellent c/p capacity have more than 10 MET's.

The lactate level in blood serum is a common parameter to asses anaerobic metabolism in patients. A high lactate level correlates with higher mortality rates and outcome.

To yet it is not clear if there exists a correlation between the preoperative cardiopulmonary capacity measured in MET's and the perioperative lactate level. We hypothysed that patients with a reduced cardiopulmonary capacity are associated with higher perioperative lactate levels, as these group of patients compensate the stressors operation/anesthesia less than patients with a good c/p capacity.

Conditions

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Sensitivity Training Groups Complication, Cardio-respiratory

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Age \> 18 years

Exclusion Criteria

* Cardiac surgery
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Witten/Herdecke

OTHER

Sponsor Role lead

Responsible Party

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Armin Zagler

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Gerhard Schneider, Prof.

Role: STUDY_CHAIR

Dept. Anaesthesiology

Locations

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Helios Klinikum Wuppertal

Wuppertal, North Rhine-Westphalia, Germany

Site Status

Countries

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Germany

Other Identifiers

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Lactate1

Identifier Type: -

Identifier Source: org_study_id