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Recruiting NCT06473922

NCT06473922 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

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Clinical Trial Summary
NCT ID NCT06473922
Status Recruiting
Phase
Sponsor Assaf-Harofeh Medical Center
Condition Tooth Extraction
Study Type OBSERVATIONAL
Enrollment 46 participants
Start Date 2024-07-01
Primary Completion 2026-05-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 85 Years
Study Type OBSERVATIONAL
Interventions
Reginal anesthesia

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 46 participants in total. It began in 2024-07-01 with a primary completion date of 2026-05-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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.

Eligibility Criteria

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. Exclusion Criteria:

Contact & Investigator

Central Contact

Sara Bar Yehuda, PhD

✉ sarabar1@shamir.gov.il

📞 972528981004

Principal Investigator

Sara Bar Yehuda, PhD

STUDY DIRECTOR

Shamir (Asaf Harofe) medical center

Frequently Asked Questions

Who can join the NCT06473922 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 85 Years, studying Tooth Extraction. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06473922 currently recruiting?

Yes, NCT06473922 is actively recruiting participants. Contact the research team at sarabar1@shamir.gov.il for enrollment information.

Where is the NCT06473922 trial being conducted?

This trial is being conducted at Be’er Ya‘aqov, Israel.

Who is sponsoring the NCT06473922 clinical trial?

NCT06473922 is sponsored by Assaf-Harofeh Medical Center. The principal investigator is Sara Bar Yehuda, PhD at Shamir (Asaf Harofe) medical center. The trial plans to enroll 46 participants.

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