Subjective Effects of Nitrous Oxide in Dental Patients - 17

NCT ID: NCT00000265

Last Updated: 2015-05-27

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

46 participants

Study Classification

OBSERVATIONAL

Study Start Date

1997-07-31

Study Completion Date

2002-01-31

Brief Summary

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The purpose of this study was to characterize mood changes during nitrous oxide inhalation in patients with different levels of preoperative dental anxiety.

Detailed Description

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Conditions

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Opioid-Related Disorders Substance-Related Disorders

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Low anxiety

No interventions assigned to this group

Moderate anxiety

No interventions assigned to this group

High anxiety

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

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Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

University of Chicago

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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James Zacny, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

University of Chicago

Locations

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University of Chicago, Anesthesia & Critical Care

Chicago, Illinois, United States

Site Status

Countries

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United States

Other Identifiers

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R01DA008391

Identifier Type: NIH

Identifier Source: secondary_id

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R01-08391-17

Identifier Type: -

Identifier Source: secondary_id

NIDA-08391-17

Identifier Type: -

Identifier Source: org_study_id

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