Evaluation of the effectiveness of aromatherapy and music on anxiety, perioperative pain and physiological parameters in patients undergoing extraction of impacted third molars

Not Applicable

Completed

• Conditions: Pain; Anxiety; Impacted third molar; Surgery - Other surgery; Anaesthesiology - Pain management; Mental Health - Anxiety; Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

• Registration Number: ACTRN12623000797673
• Lead Sponsor: Ana Rocío García Carricondo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-07-26
• Study Completion: 2023-09-21
• Last Update Posted: 15 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 273

Inclusion Criteria

1. Adult patients between 18-50 years of age (age at which the eruption or the pathologies derived from the lack of eruption occures)
2. Both men and women will be selected
3. Single procedure per surgical act, that is, only one extraction per patient and episode.
4. Procedure performed under exclusive local anesthesia.
5. Patients who agree to participate in the study and sign the Informed Consent form.; 1. Adult patients between 18-50 years of age (age at which the eruption or the pathologies derived from the lack of eruption occures)
2. Both men and women will be selected
3. Single procedure per surgical act, that is, only one extraction per patient and episode.
4. Procedure performed under exclusive local anesthesia.
5. Patients who agree to participate in the study and sign the Informed Consent form.

Exclusion Criteria

1. Patients under 18 years of age or over 50 years of age.
2. Multiple procedure, that is, dental polyextraction in the same surgical act.
3. Patients with deafness or with hearing pathology.
4. Patients with anosmia or significant loss of smell.
5. Patients who suffer from epilepsy or have had an epileptic seizure in the last 6 months.
6. Anticoagulated patients or with bleeding disorders.
7. Patients undergoing cancer treatment or immunosuppressed.
8. Patients being treated with bisphosphonates.
9. Patients with systemic pathology that may interfere with the result.
10. Patients who have received locoregional radiotherapy.
11. Previous surgery in the lower retromolar trigone area.
12. Disabled patients, non-collaborators.
13. Patients unable to understand and fill in the visual analog scale and the anxiety questionnaire.
14. Patients operated under general anesthesia and / or sedation.
15. Presence of active suppurative infection at the time of surgery.
16. Pregnant patients or possibility of pregnancy (verified by pregnancy test).
17. Patient who does not want or authorize to participate in the study or does not have a correct command or understanding of the Spanish language.
18. Patients with severe cardiac impulse conduction dysfunctions.
19. Patients with decompensated heart failure.; 1. Patients under 18 years of age or over 50 years of age.
2. Multiple procedure, that is, dental polyextraction in the same surgical act.
3. Patients with deafness or with hearing pathology.
4. Patients with anosmia or significant loss of smell.
5. Patients who suffer from epilepsy or have had an epileptic seizure in the last 6 months.
6. Anticoagulated patients or with bleeding disorders.
7. Patients undergoing cancer treatment or immunosuppressed.
8. Patients being treated with bisphosphonates.
9. Patients with systemic pathology that may interfere with the result.
10. Patients who have received locoregional radiotherapy.
11. Previous surgery in the lower retromolar trigone area.
12. Disabled patients, non-collaborators.
13. Patients unable to understand and fill in the visual analog scale and the anxiety questionnaire.
14. Patients operated under general anesthesia and / or sedation.
15. Presence of active suppurative infection at the time of surgery.
16. Pregnant patients or possibility of pregnancy (verified by pregnancy test).
17. Patient who does not want or authorize to participate in the study or does not have a correct command or understanding of the Spanish language.
18. Patients with severe cardiac impulse conduction dysfunctions.
19. Patients with decompensated heart failure.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
evel of perioperative anxiety assessed by the State and Trait Anxiety Inventory (STAI)[ 20 minutes Pre and 20 minutes Post-operative];Level of perioperative pain assessed by 100 mm VAS scale[ Patient will fill in the VAS scale 20 minutes after the intervention, indicating the pain felt during the surgery];Level of perioperative anxiety assessed by the State and Trait Anxiety Inventory (STAI)[ 20 minutes Pre and 20 minutes Post-operative];Level of perioperative pain assessed by 100 mm VAS scale[ Patient will fill in the VAS scale 20 minutes after the intervention, indicating the pain felt during the surgery]