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Active, not recruitingNCT07041879Updated Dec 16, 2025

Piezotome Atraumatic Tooth Extraction And Immediate Implant Placement In Maxillary Anterior Region

An interventional study of maxillary anterior teeth atraumatically extracted with piezotome extraction kit, and subsequent immediate implant placement and maxillary anterior teeth atraumatically extracted with periotome, and subsequent immediate implant placment in Piezotome and Implant-supported Single Crowns, sponsored by Alexandria University. Active, not recruiting at 1 site in Egypt. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-12-16.

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

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Oct 2024, registered May 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Tooth extraction is critical for dental treatment complications followed by immediate implant placement to restore the extracted tooth . The use of devices or instruments such as piezotome and periotome as aids in atraumatic surgical proceduresو conserving both bone and soft tissue, allowing extraction without unnecessary socket expansion. Immediate implant placement into fresh extraction sockets offers some esthetic and functional advantages.

the Aim of this study is to compare and evaluate the effectiveness of the piezotome and periotome as aids for atraumatic extraction in immediate implant placement in maxillary anterior teeth.

Read the detailed description

30 patients with non-restorable maxillary anterior teeth will be included. Teeth will be extracted using an atraumatic tooth extraction using piezotome and periotome as aids in atraumatic surgical procedures. After that an immediate implant will be placed into the fresh extraction socket . patients will be recalled for follow-up 3months after implant placement to evaluate pain by VAS and evaluate bone healing using CBCT.

02

Conditions studied

  • Piezotome
  • Implant-supported Single Crowns

Keywords

  • tooth extraction
  • immediate implant
  • bone healing
  • piezotome
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 and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patients of both gender with a non-restorable maxillary anterior tooth in the aesthetic zone indicated for extraction and subsequent immediate implant placement. Including those with:

    1. Severely carious tooth that it cannot be restored.
    2. Pulpal necrosis or irreversible pulpitis that is not amenable to endodontics.
    3. Periodontally involved Tooth with grade 2 mobility or above.
    4. Tooth with root caries that can't be restored.
  2. Patients with extraction socket Type I, according to Elian's classification

Exclusion criteria

Exclusion Criteria:

  1. Patients with extraction socket Type II or III, with defect in the buccal plate
  2. Patients with deciduous teeth.
  3. Heavy smokers.
  4. Medically compromised patients with conditions that would impede implant osteointegration and healing.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (estimated)

Study arms

  • Active comparator
    Atraumatic extraction with piezotome and subsequently immediate implant placement

    Patients with maxillary anterior teeth will be atraumatically extracted with piezotome extraction, and subsequently immediate implant placement

    Procedure: maxillary anterior teeth atraumatically extracted with piezotome extraction kit, and subsequent immediate implant placement

  • Experimental
    Atraumatic extraction with periotome and subsequently immediate implant placement

    Patients with maxillary anterior teeth will be atraumatically extracted with periotome, and subsequently immediate implant placement

    Procedure: maxillary anterior teeth atraumatically extracted with periotome, and subsequent immediate implant placment

Interventions

  • Proceduremaxillary anterior teeth atraumatically extracted with piezotome extraction kit, and subsequent immediate implant placement

    piezotome extraction kit,

  • Proceduremaxillary anterior teeth atraumatically extracted with periotome, and subsequent immediate implant placment

    periotome

06

What researchers measure

Primary outcomes

  1. Radiographic assessment of the management of the crestal bone width and changes in labial bone thickness.

    A postoperative CBCT will be taken within 24 hours of implant placement followed by a 6-months scan, and values will be compared with the preoperative record. The assessment will be conducted using the tools on the "On Demand 3D App." Software\*. The following criteria will be assessed:

    Time frame: 5 months

Secondary outcomes

  1. Clinical Wound Healing

    All patients will be recalled for a clinical follow-up period at 7, 14, and 21 days postoperative for the assessment of Wound healing using the Pink Esthetic Score (PES)

    Time frame: 21 days

07

Study locations

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

References and documents

Individual participant data

Plan to share: No — all data will be de-identified to protect the participant data. patients signed an informed consent for the use of their medical records and data for study

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 16, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07041879
Lead sponsor
Alexandria University
Responsible party
Sponsor
First posted
Jun 27, 2025
Start date
Oct 1, 2024
Primary completion
Sep 30, 2025
Completion
Mar 30, 2026 (estimated)
Last update
Dec 16, 2025

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 active, not recruiting, as verified in May 2025. You cannot join it, but the record below documents what was studied.

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