Skip to content

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

Piezotome Atraumatic Tooth Extraction And Immediate Implant Placement In Maxillary Anterior Region: Randomized Clinical Trial

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07041879
Enrollment
30
Registered
2025-06-27
Start date
2024-10-01
Completion date
2026-03-30
Last updated
2025-12-16

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

Conditions

Implant-supported Single Crowns, Piezotome

Keywords

tooth extraction, immediate implant, bone healing, piezotome

Brief 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.

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.

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

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Sequentially numbered, opaque, sealed envelopes (SNOSE) allocation concealment method will be utilized. Each participant included in the study will be given a serial number that will be used in the allocation. These numbers will be written in identical sheets of paper with the group to which each participant is allocated and placed inside opaque envelopes carrying the respective names of participants. A trial independent personnel will be assigned the role of keeping the envelopes and unfolding them only at the time of the operation, so that the participant is allocated to a group which is concealed from the operator

Intervention model description

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

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

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.

Design outcomes

Primary

MeasureTime frameDescription
Radiographic assessment of the management of the crestal bone width and changes in labial bone thickness.5 monthsA 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:

Secondary

MeasureTime frameDescription
Clinical Wound Healing21 daysAll 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)

Countries

Egypt

Outcome results

None listed

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