Effectiveness of Respirators Fit Factor in Healthcare Providers With and Without Beard

NCT ID: NCT04391010

Last Updated: 2020-06-02

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

Clinical Phase

NA

Total Enrollment

63 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-05-22

Study Completion Date

2020-06-01

Brief Summary

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The study aim will be to determine the fit factor of surgical masks and filtering respirators in healthcare providers with and without beard. A randomized clinical trial will be carried out recruiting a sample of 52 healthcare providers with and without beard. Fit factor will be measured with both surgical masks and filtering respirators and compared between healthcare providers with and without beard.

Detailed Description

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Conditions

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Community Health Workers Filtration Masks

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Health care providers with beard

Group Type OTHER

Surgical masks

Intervention Type OTHER

Surgical masks will be applied in health care providers

Filtering respirators

Intervention Type OTHER

Filtering respirators will be applied in health care providers

Health care providers without beard

Group Type OTHER

Surgical masks

Intervention Type OTHER

Surgical masks will be applied in health care providers

Filtering respirators

Intervention Type OTHER

Filtering respirators will be applied in health care providers

Interventions

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Surgical masks

Surgical masks will be applied in health care providers

Intervention Type OTHER

Filtering respirators

Filtering respirators will be applied in health care providers

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Healthcare providers

Exclusion Criteria

* Pulmonary diseases
* Pregnant women
* Not sign the informed consent form
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universidad Complutense de Madrid

OTHER

Sponsor Role lead

Responsible Party

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César Calvo Lobo

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Universidad Complutense de Madrid

Madrid, , Spain

Site Status

Countries

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Spain

Other Identifiers

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UCM Respirators Fit Factor

Identifier Type: -

Identifier Source: org_study_id

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