Audiological Evaluation of Anesthetists

January 8, 2018 updated by: khaled salah mohamed, Assiut University

the Effects of Noise in Operating Rooms on Anesthetists Hearing

The investigators aim to investigate the effect of operating room noise on anesthetist hearing

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Egypt
      • Assiut, Egypt, 71515
        • Assiut university hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

28 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

anesthetist doctor who subject to noise in operating rooms

Description

Inclusion Criteria:

  • anesthetist doctor and non-anesthetist doctor less than 40 years

Exclusion Criteria:

  • doctors above 40 years

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
anesthetist group
anesthetist doctor who subjected to noise in operating rooms
control group
doctors in the same hospital who are not subjected to noise in operating rooms

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Extended high frequency audiometry
Time Frame: 20 minutes
pure tone audiometry in the frequency range from 250Hz-20,000Hz
20 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Transient Evoked Otoacoustic Emission
Time Frame: 10 minutes
stimulus induced cochlear echos in the frequency range from 1000-4000 Hz
10 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Assiut University

Investigators

  • Principal Investigator: Khaled Salah Mohamed, MD, Assiut University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 10, 2017

Primary Completion (Actual)

January 8, 2018

Study Completion (Actual)

January 8, 2018

Study Registration Dates

First Submitted

April 9, 2017

First Submitted That Met QC Criteria

April 14, 2017

First Posted (Actual)

April 18, 2017

Study Record Updates

Last Update Posted (Actual)

January 9, 2018

Last Update Submitted That Met QC Criteria

January 8, 2018

Last Verified

January 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • kmohamed

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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