Assessing Levels of Fear and Anxiety and Monitoring Wound Healing Among Patients Who Are About to Undergo Wisdom Tooth Extraction Surgery or Jaw Implant Surgery Under Local Anesthesia Versus General Anesthesia

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorAssaf-Harofeh Medical Center

About this trial

Tooth extraction is one of the most common surgical procedures in dentistry. Up to 15% of the world's adult population suffers from high anxiety about dental treatments. The stress resulting from this anxiety may cause a delay in the healing and fusion of the surgical wound. Therefore, it is possible to perform this surgical tooth extraction procedure under general anesthesia.

The purpose of the present study is to assess the level of anxiety/fear and to monitor the wound healing process among patients who are about to undergo surgery to remove wisdom teeth or no more than 3 jaw implants under local anesthesia in the dental clinic compared to patients who are about to undergo the same surgery under general anesthesia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Male and females, over 18 years of age who about to undergo surgery to extract wisdom teeth or no more than 3 implants in the jaw under local anesthesia in the dental clinic or under general anesthesia in a hospital operating room.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Reginal anesthesia

    Procedure/Surgery

    General anesthesia

Treatment groups

46 Participants
are divided into 2 treatment groups
Group A: General anasthesia1 intervention
Group B: Regional anesthesia1 intervention

Trial outcomes

Primary outcomes

1

Level of fear

Level of fear from pain and dental fear will be monitored by questionnaireד

Time frame
From visit 1 which will be 5-7 days before surgery to visit 5 which will be 6 weeks after surgery
2

Wound healing

Will be monitored by the IPR questionnaire

Time frame
From visit 3 which will be 5 days after surgery to visit 5 which will be 6 weeks after surgery

Secondary outcomes

Other outcomes

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