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The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Saturation Levels

NCT ID: NCT00854048

Last Updated: 2016-11-30

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

66 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-12-31

Study Completion Date

2008-07-31

Brief Summary

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Evaluate pulse oximeters with children after cardiopulmonary by-pass under low Oxygen conditions.

Detailed Description

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Conditions

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Cardiopulmonary Bypass

Keywords

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Pediatric Oxygen Saturation Cardiopulmonary bypass

Study Design

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Observational Model Type

CASE_CROSSOVER

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Include pediatric patients with a baseline Sa02 \< 90% and no contraindications to using an adhesive sensor.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medtronic - MITG

INDUSTRY

Sponsor Role collaborator

Ulf Borg

INDUSTRY

Sponsor Role lead

Responsible Party

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Ulf Borg

Director Clinical Science

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Xu Feng, MD

Role: PRINCIPAL_INVESTIGATOR

Children's Hospital Congqing Medical University

Locations

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Chidren's Hospital

Chongqing University of Medical Sciences, Chongqing Municipality, China

Site Status

Countries

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China

Other Identifiers

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M112

Identifier Type: -

Identifier Source: org_study_id