Oral Care Study on Burn Patients

NCT ID: NCT01302457

Last Updated: 2016-10-13

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WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2007-09-30

Study Completion Date

2013-09-30

Brief Summary

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There have been multiple articles done regarding oral hygiene on patients in burn and intensive care patients. All articles agree the need for good oral hygiene in these special needs patients. They also note that more research needs to be done on this subject, yet have no direction of how to proceed in this research. Currently, no research has been done on the burn/intensive care patient to see if there is a difference form the non-hospitalized patient which oral hygiene protocol is based on.

Detailed Description

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BACKGROUND IMFORATION AND INTRODUCTION There have been multiple articles done regarding oral hygiene on patients in burn and intensive care patients. All articles agree the need for good oral hygiene in these special needs patients. They also note that more research needs to be done on this subject, yet have no direction of how to proceed in this research. Currently, no research has been done on the burn/intensive care patient to see if there is a difference form the non-hospitalized patient which oral hygiene protocol is based on.

OJECTIVE The primary purpose of this prospective study is to determine if the burn/intensive care patient's oral condition is similar or different from the normal standard.

PATIENT SELECTION CRITERIA

1. Patients age must be 19 and older.
2. Patients must be on a ventilator in the burn or intensive care unit.
3. The control group will be 19 years or older and be randomly picked from from volunteer staff at Saint Elizabeth Regional Medical Center.

DESIGN This is a prospective study that will look at the similarities and difference of both groups. This will help us determine if there is a need to improve oral hygiene protocol given to burn/intensive care patients. Each group will consist of 25 subjects

Conditions

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Burn

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Healthy Same Subjects

The control group will be 19 years or older and be randomly picked from from volunteer staff at Saint Elizabeth Regional Medical Center. This is a prospective study that will look at the similarities and difference of both groups. This will help us determine if there is a need to improve oral hygiene protocol given to burn/intensive care patients. Each group will consist of 25 subjects

No interventions assigned to this group

Health Volunteers

The control group will be 19 years or older and be randomly picked from volunteer staff at Saint Elizabeth Regional Medical Center.

DESIGN This is a prospective study that will look at the similarities and difference of both groups. This will help us determine if there is a need to improve oral hygiene protocol given to burn/intensive care patients. Each group will consist of 25 subjects

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Patients age must be 19 and older.
2. Patients must be on a ventilator in the burn or intensive care unit.
3. The control group of Healthy Volunteers will be 19 years or older and be randomly picked from volunteer staff at Saint Elizabeth Regional Medical Center.

Exclusion Criteria

* Unable to complete Informed Consent Process
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Saint Elizabeth Regional Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Saint Elizabeth Regional Medical Center

Principal Investigators

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Brian Burgess, D.D.S.

Role: PRINCIPAL_INVESTIGATOR

Saint Elizabeth Regional Medical Center

Locations

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Saint Elizabeth Regional Medical Center

Lincoln, Nebraska, United States

Site Status

Countries

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United States

Other Identifiers

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609-036

Identifier Type: -

Identifier Source: org_study_id

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