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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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06473922
Enrollment
46
Registered
2024-06-25
Start date
2024-07-01
Completion date
2026-08-30
Last updated
2024-06-25

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

Conditions

Tooth Extraction

Brief summary

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.

Detailed description

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. The various measurements of the study will include: Level of free cortisol hormone in saliva.The levels of this hormone are correlated to the level of fear The level of fear of pain will be measured using the Fear of Pain Questionnaire - (FPQ-III) The level of fear of dental pain will be measured using the short version of the fear of dental pain questionnaire - FDPQ Level of dental anxiety - will be measured using by the dental anxiety scale of The DAS Corah . To monitor the inflammation and wound healing, the inflammatory proliferation scale (IPR) will be used to monitor the wound healing process The study includes 5 visits: Visit 1: 5-7 days before surgery - in the waiting room of the dental clinic. The patients will sign an informed consent form, fill out questionnaires and a saliva test will be taken from them. A clinical assessment will be conducted by the surgeon Visit 2: on the day of surgery, in the waiting room of the dental clinic or the operating room (depending on the type of anesthesia planned). The patients will fill out questionnaires and a saliva sample will be taken from them Visit 3: 5 days after the surgery - in the waiting room of the dental clinic The patients will fill out questionnaires and a saliva sample will be taken from them. The surgeon will report complications and complete the IPR. Visit 4: 14 days after surgery The surgeon will complete the IPR. Visit 5: 6 weeks after surgery The surgeon will complete the IPR.

Interventions

PROCEDUREReginal anesthesia

General anesthesia

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years

Inclusion criteria

Age - from ≥ 18 years, ASA 1- or 2, Signing a written informed consent before starting all procedures related to the research, Ability to cooperate with the researcher and meet the research requirements.

Design outcomes

Primary

MeasureTime frameDescription
Level of fearFrom visit 1 which will be 5-7 days before surgery to visit 5 which will be 6 weeks after surgeryLevel of fear from pain and dental fear will be monitored by questionnaireד
Wound healingFrom visit 3 which will be 5 days after surgery to visit 5 which will be 6 weeks after surgeryWill be monitored by the IPR questionnaire

Countries

Israel

Contacts

Primary ContactSara Bar Yehuda, PhD
sarabar1@shamir.gov.il972528981004
Backup ContactZoya Haitov Ben Zikri, MD
ZoyaC@shamir.gov.il972537346186

Outcome results

None listed

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