Emotional and Oral Characteristics of Patients That Attend a Dental Consultation for the Extraction of Third Molars

NCT ID: NCT06388265

Last Updated: 2025-11-19

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

82 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-09

Study Completion Date

2025-07-31

Brief Summary

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Analyze the level of anxiety, hemodynamic parameters, oral status, and satisfaction among patients undergoing third molar extraction, we will assess those who attend the Master of Oral Medicine, Surgery, and Implantology program at the University of Barcelona.

Detailed Description

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Conditions

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Anxiety and Fear

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Caregivers

Study Groups

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Verbal and Written detailed information

The experimental group will receive verbal information about the procedure (exodontia of third molars) and additionally a trifold with detailed information about the surgical procedure.

Group Type EXPERIMENTAL

Trifold information

Intervention Type OTHER

Additional detailed and written information about the procedure will be given to the participants

Control

The control group will only receive verbal information about the surgical procedure.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Trifold information

Additional detailed and written information about the procedure will be given to the participants

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Individuals 18 years old or older, from both genders that wished to voluntarily participate in the study and that required the extraction of third molars.

Exclusion Criteria

* Systemic diseases (ASA III or IV) that contraindicate the performance of the surgical procedure
* Pregnant women
* Individuals that did not understand and/or could not respond the given questionnaire.
* Patients that required the extraction of a different tooth than a third molar or that required the extraction of more than two third molars in the same surgical time.
* Patients who had undergone extraction of a third molar in the twelve months prior to the current visit.
* Patients taking antidepressant medication or anxiolytic medication
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Barcelona

OTHER

Sponsor Role lead

Responsible Party

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Mayra Schemel Suarez

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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José López-López, PhD

Role: STUDY_DIRECTOR

University of Barcelona

Mayra Schemel Suarez, DDS

Role: PRINCIPAL_INVESTIGATOR

University of Barcelona

Locations

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Hospital Odontològic Universitat de Barcelona

L'Hospitalet de Llobregat, Barcelona, Spain

Site Status

Countries

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Spain

Other Identifiers

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18/2018, Acta 26-6-2018

Identifier Type: -

Identifier Source: org_study_id

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