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CompletedNCT07297043Updated Dec 29, 2025

Efficacy of Er:YAG Laser in Removing Impacted Mandibular Third Molars

An interventional study of Er:YAG laser and Conventional Rotary Instruments Surgery in Impacted Mandibular Third Molar, sponsored by Alexandria University. Completed at 1 site in Egypt. Open to participants aged 18 Years to 30 Years. Per ClinicalTrials.gov, last updated 2025-12-29.

Sponsored by Alexandria University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 2 months after the study started (first participant enrolled Sep 2024, registered Dec 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

This randomized controlled clinical trial aims to evaluate the efficacy of the Er:YAG laser in the removal of impacted mandibular third molars compared to the conventional surgical technique. The study assesses surgical efficiency, postoperative pain, swelling, trismus, and overall patient recovery. The goal is to determine whether the Er:YAG laser provides a safer and less traumatic alternative to traditional bone-cutting methods during third molar surgery.

Read the detailed description

Impacted mandibular third molars are among the most commonly extracted teeth, and conventional surgical removal often involves bone cutting using rotary instruments, which may increase postoperative morbidity. Laser-assisted surgery, particularly using the Er:YAG laser, has been proposed as a minimally invasive alternative with potential benefits such as reduced thermal damage, improved healing, and less postoperative discomfort.

This study compares Er:YAG laser-assisted bone removal with the conventional bur technique in terms of operative time, intraoperative ease, and postoperative outcomes including pain, edema, and trismus. Patients meeting the eligibility criteria are randomly allocated into two groups: a laser-assisted surgery group and a conventional surgery group. Standardized measurements and follow-up assessments are conducted to evaluate clinical outcomes and determine the effectiveness and safety of the Er:YAG laser in third molar surgery.

02

Conditions studied

  • Impacted Mandibular Third Molar

Keywords

  • Third Molar Surgery
  • Er:YAG Laser
  • Laser-Assisted Surgery
  • Oral Surgery
03

In context

Lead sponsor

Alexandria University is the lead sponsor of 569 studies on the registry; 125 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

    • Adults aged 20-30 years requiring surgical extraction of a mesioangular impacted mandibular third molar.

      • Healthy individuals with no systemic diseases that may influence bone metabolism or wound healing.
      • Good oral hygiene and absence of local infection at the surgical site.
      • No contraindications to local anesthesia, surgical extraction, or use of the Er:YAG laser.
      • Radiographic evidence confirming normal bone structure without cysts or pathological lesions.
      • Willingness to participate and ability to provide informed consent.

Exclusion criteria

Exclusion Criteria:

    • Systemic medical conditions affecting bone healing or postoperative response (e.g., uncontrolled diabetes, immunodeficiency, metabolic bone disorders).

      • Current or recent use of medications influencing bone remodeling (e.g., bisphosphonates, corticosteroids, immunosuppressants).
      • Heavy smoking (>10 cigarettes/day).
      • Pregnant or breastfeeding females.
      • Poor oral hygiene, active infection, or pericoronitis at the surgical site.
      • Previous surgery, trauma, or pathology in the mandibular third molar region.
      • Known allergies or contraindications to any material or procedure used in the study.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Experimental
    Er:YAG Laser Group

    Participants in this group will undergo impacted mandibular third molar surgery using the Er:YAG laser for bone removal.

    Device: Er:YAG laser

  • Active comparator
    Conventional Rotary Instrument Group

    Participants in this group will undergo impacted mandibular third molar surgery using conventional rotary instruments (bur and handpiece) for bone cutting.

    Procedure: Conventional Rotary Instruments Surgery

Interventions

  • DeviceEr:YAG laser

    Er:YAG laser (2940 nm) used for bone cutting during impacted mandibular third molar surgery.

  • ProcedureConventional Rotary Instruments Surgery

    Conventional rotary instruments used for bone removal during surgical extraction of impacted mandibular third molars.

06

What researchers measure

Primary outcomes

  1. Postoperative Pain Score

    Postoperative pain will be assessed using a Visual Analog Scale (VAS) ranging from 0 (no pain) to 10 (worst pain) at postoperative intervals.

    Time frame: Immediate postoperative, 24 hours, 3 days, and 7 days

Secondary outcomes

  1. Postoperative Swelling

    Facial swelling will be measured using linear facial measurements (tragus-pogonion and gonion-pogonion distances) preoperatively and at postoperative intervals.

    Time frame: Immediate postoperative, 24 hours, 3 days, and 7 days

  2. Postoperative Trismus

    Maximum interincisal mouth opening will be measured in millimeters preoperatively and at postoperative intervals to assess trismus.

    Time frame: Immediate postoperative, 24 hours, 3 days, and 7 days

  3. Bone Density

    Bone density at the extraction site will be assessed using standardized digital radiographs. Gray-scale values will be measured at predetermined reference points to compare bone healing between groups.

    Time frame: Immediate postoperative, 1 month, and 3 months

07

Study locations

1 site
  • Faculty of Dentistry, Alexandria University
    Alexandria, Alexandria Governorate, Egypt
08

References and documents

Publications

  • Elhaw KA, Abdelhakim AA, Dominguez J A, Eldibany RM, Tost A E. Efficacy of Er:YAG laser in removal of impacted mandibular third molars (a randomized controlled clinical trial). BMC Oral Health. 2026 Jun 5;26(1):1060. doi: 10.1186/s12903-026-08790-w. PubMed 42243813 ↗

Individual participant data

Plan to share: Undecided — The plan for sharing individual participant data (IPD) has not yet been determined. Decisions regarding IPD sharing will depend on institutional policies, ethical approvals, and future publication requirements.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 29, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07297043
Lead sponsor
Alexandria University
Responsible party
Karim Anwer Ahmed Nazmy (Postgraduate Researcher, Oral Laser Applications, Alexandria University) — Principal investigator
First posted
Dec 22, 2025
Start date
Sep 25, 2024
Primary completion
Jan 15, 2025
Completion
Jan 29, 2025
Last update
Dec 29, 2025

Study contacts

Karim Elhaw, MSc (Oral Laser Applications)
principal investigator · Alexandria University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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