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Clinical Trials/NCT06589908
NCT06589908CompletedNot Applicable

Evaluation of the Use of RELAX Glasses on Anxiety of Patients Undergoing Dental Extraction > 2 Teeth, Under Local Anesthesia, Compared With Those Not Using Glasses

Centre Hospitalier de Valenciennes1 site in 1 country106 target enrollmentStarted: August 31, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
106
Locations
1
Primary Endpoint
Change from baseline in visual analogue scale anxiety scores after tooth extraction

Study Overview

Brief Summary

The vast majority of tooth extraction surgery is performed under local anaesthetic, and can be a source of anxiety. In their 2015 article, Appukuttan et al studied the anxiety felt by 1148 patients prior to tooth extraction, and reported up to 82% of patients anxious before a procedure.

In 2020, Yamashita et al demonstrated the value of virtual reality in reducing patient anxiety during the extraction of three impacted mandibular molars, with no clear effect on the pain felt by the patient.

The use of a virtual reality headset has been shown to reduce anxiety in dental surgery or in hand surgery under local anesthesia with the WALANT technique. On the other hand, virtual reality and the use of 3D can cause discomfort and side effects such as nausea and dizziness. Audiovisual distraction is also known to be effective in reducing pain and anxiety in patients, with fewer side effects.

The investigators have therefore chosen to use RELAX® eyewear. They wish to study its effect on anxiety, pain and overall patient and surgeon satisfaction.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
14 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patient undergoing dental extraction > 2 teeth under local anesthesia;
  • •Over 14 years of age on the day of inclusion;
  • •Patient with written consent or additional parental consent for minors;
  • •Socially insured patient;
  • •Patient willing to comply with all study procedures and duration.

Exclusion Criteria

  • •Medical history contraindicating RELAX glasses
  • •Known and current abuse of alcohol and/or illicit drugs that may interfere with patient safety and/or compliance;
  • •Any condition that would render the patient unfit for the study: current presence of cognitive disorders (MMS < 15), severe psychiatric disorders (bipolar disorders, psychotic disorders according to DSM-V classification);
  • •Major anxiety requiring preoperative anxiolytics;
  • •Patient under court protection;
  • •Patient participating in another study;
  • •Patient's refusal to use glasses;
  • •Visually impaired or blind patient.

Arms & Interventions

Group with RELAX glasses

Experimental

Behavioral : RELAX glasses Glasses which are a solution of audiovisual sedation by positive distraction for hospital medical use

Intervention: RELAX glasses (Behavioral)

Group without RELAX glasses

No Intervention

Outcomes

Primary Outcomes

Change from baseline in visual analogue scale anxiety scores after tooth extraction

Time Frame: In the 5 minutes after the end of surgery

The visual analogue anxiety scale from 0 to 10, with meaning no anxiety and 10 very high anxiety

Secondary Outcomes

  • Variation in pain between entering and leaving the surgical technical platform between the 2 arms using a visual analogue scale(In the 5 minutes after the end of surgery)
  • Rate of patients receiving at least one analgesic(After local anesthesia)
  • Overall satisfaction between the group using RELAX glasses and the group following the usual course (without RELAX glasses) measured by a visual analogue scale(Immediative postoperative)
  • Surgeon's satisfaction with the feasibility of the procedure in a patient wearing RELAX glasses filling in a self-assessment questionnaire(Immediative postoperative)
  • Pre-existing anxiety, only in patients receiving RELAX glasses, measured with the STAI-YB score(7 days (+/-3 days) after surgery)
  • Evaluation of the impact of patient agitation on the operative procedure by filling in a self-assessment questionnaire after each operative procedure.(Immediative postoperative)
  • Overall satisfaction between the group using RELAX glasses and the group following the usual course (without RELAX glasses) measured by a visual analogue scale(Immediative postoperative)
  • Surgeon's satisfaction with the feasibility of the procedure in a patient wearing RELAX glasses filling in a self-assessment questionnaire(Immediative postoperative)
  • Pre-existing anxiety, only in patients receiving RELAX glasses, measured with the STAI-YB score(7 days (+/-3 days) after surgery)
  • Variation in pain between entering and leaving the surgical technical platform between the 2 arms using a visual analogue scale(In the 5 minutes after the end of surgery)
  • Rate of patients receiving at least one analgesic(After local anesthesia)
  • Evaluation of the impact of patient agitation on the operative procedure by filling in a self-assessment questionnaire after each operative procedure.(Immediative postoperative)

Investigators

Sponsor Class
Network
Responsible Party
Sponsor

Study Sites (1)

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