Agreement of the Nexfin™ Monitor With Non-invasive Blood Pressure Measurement

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

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-05-31

Study Completion Date

2016-01-31

Brief Summary

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Currently, BP is measured using an inflatable cuff wrapped around the patient's upper arm. This can be set to inflate every minute, but measurement may fail due to patient movement or shivering. Failed measurement occurs in up to 38% of patients.

This study aims to determine how the Nexfin device - which measures BP using a cuff wrapped around a finger - compares to standard BP measurement.

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Detailed Description

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This study aims to determine how the Nexfin device - which measures BP using a cuff wrapped around a finger - compares to standard BP measurement.

Conditions

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Blood Pressure Measurement

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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study group

all participants

Nexfin

Intervention Type DEVICE

Nexfin cuff placed on finger to measure blood pressure

Interventions

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Nexfin

Nexfin cuff placed on finger to measure blood pressure

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Healthy female pregnant patients
* ≥19 years old
* Undergoing elective Cesarean section under spinal or combined spinal-epidural anesthesia

Exclusion Criteria

* Contraindication to wearing Nexfin cuff (upper limb vascular disease, amputated digits)
* Obesity (BMI \> 38 kg/m2)
* Use of arterial line for BP measurement
* Inability to read and understand English

Minimum Eligible Age

19 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes