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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06388265
Enrollment
82
Registered
2024-04-29
Start date
2022-01-09
Completion date
2025-07-31
Last updated
2025-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety and Fear

Brief summary

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.

Interventions

OTHERTrifold information

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

Sponsors

University of Barcelona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Changes in STAI-SThrough study completion, an average of 5 weeksThe Anxiety State scale (S-Anxiety) is an inventory that has been validated and assesses the current state of anxiety of the participant measured through an auto evaluation, asking how the evaluated individual feels in this moment, using items that measure subjective feelings of apprehension, tension, nervousness, worry and activation/excitement of the autonomic nervous system. The total scores can go from 20 to 80 points A cut point value of 39 to 40 points has been suggested to detect clinically significant symptoms in the Anxiety State scale. STAI-S will be assessed in 4 stages: 1. At the initial consultation (baseline) 2. Immediately before the procedure and administration of the local anaesthetic solution 3. Immediately after the procedure is completed 4. 1 week after the procedure (exodontia)
Changes in MDASup to 3 weeksThe modified dental anxiety scale (MDAS) is an auto evaluation questionnaire about dental anxiety that contains 5 items, each one with 5 possible answers that reflects in order an increase of anxiety (no anxiety to extremely anxious). The total score can go from 5 points to a maximum of 25 points. The lower limit to define an individual with extreme anxiety is 19 points and to define the presence of anxiety the score must be higher than 10 points. MDAS will be assessed in 2 stages: 1. At the initial consultation (baseline) 2. Immediately before the procedure and administration of the local anaesthetic solution

Secondary

MeasureTime frameDescription
Changes in blood pressureThrough study completion, an average of 5 weeksChanges in Blood pressure (Systolic and dyastolic) measured in mmHg Blood pressure will be assessed in 5 stages: 1. At the initial consultation (baseline) 2. Immediately before the procedure and administration of the local anaesthetic solution 3. Immediately after administration of the local anaesthetic solution 4. Immediately after the procedure is completed
Changes in Heart rateThrough study completion, an average of 5 weeksChanges in heart rate measured in beats per minute Heart rate will be assessed in 5 stages: 1. At the initial consultation (baseline) 2. Immediately before the procedure and administration of the local anaesthetic solution 3. Immediately after administration of the local anaesthetic solution 4. Immediately after the procedure is completed
Changes in Oxygen saturationThrough study completion, an average of 5 weeksChanges in oxygen saturation measured in percentage (%) Oxygen saturation will be assessed in 5 stages: 1. At the initial consultation (baseline) 2. Immediately before the procedure and administration of the local anaesthetic solution 3. Immediately after administration of the local anaesthetic solution 4. Immediately after the procedure is completed
Patient Satisfaction of procedure1 week after the procedureA questionnaire will be provided to the participants that consists of 6 questions, 2 questions to know the degree of discomfort at the last visit (suture removal control post exodontia) with 4 possible answers: none, little, moderate, a lot; and 4 questions to determine the degree of satisfaction with all the dental treatment carried out with affirmative or negative answers

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026