Evaluation the Accuracy of Immediate Implant Placement Using SocketFit Static Surgical Guide Versus Conventional Static Surgical Guide in Anterior Esthetic Zone (SocketFit)
11. august 2026 opdateret af: Aliaa Saeed Kishk, Tanta University
This study compares two types of surgical guides used during immediate dental implant placement in the upper front teeth.
One guide is a conventional static surgical guide, while the other is a modified SocketFit static surgical guide designed to improve stability after tooth extraction.
The purpose of the study is to determine whether the SocketFit guide improves the accuracy of implant placement.The findings may help improve the precision and predictability of immediate dental implant treatment in the anterior esthetic zone.
Studieoversigt
Status
Rekruttering
Intervention / Behandling
Detaljeret beskrivelse
Immediate implant placement in the anterior esthetic zone is a predictable treatment option that reduces treatment time and preserves peri-implant soft and hard tissues.
Static computer-guided surgery has improved the accuracy of implant placement; however, guide stability may be compromised immediately after tooth extraction because of complex morphology and angulation of post-extraction sockets, as well as variations in bone density.These factors can lead to surgical drill displacement, causing the implant to deviate from its intended trajectory.Therefore, The SocketFit static surgical guide incorporates a socket-engaging extension designed to enhance guide seating and stability during osteotomy preparation.
Limited evidence is available regarding the accuracy of this modified guide compared with the conventional tooth-supported static surgical guide.
Therefore, this study aims to evaluate the accuracy of immediate implant placement using the SocketFit static surgical guide versus the conventional static surgical guide in the anterior esthetic zone.
Accuracy will be assessed by comparing the planned and actual implant positions using postoperative Cone Beam Computed Tomography (CBCT) superimposition, evaluating coronal, apical, angular, and depth deviations.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
26
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Aliaa s. Kishk, Batchelor
- Telefonnummer: +201015101949
- E-mail: Aliaa8271staff@dent.tanta.edu.eg
Undersøgelse Kontakt Backup
- Navn: rehab f ghouraba, PHD
- Telefonnummer: +201211512429
- E-mail: rehab_ghouraba@dent.tanta.edu.eg
Studiesteder
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Gharbia Governorate
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Tanta, Gharbia Governorate, Egypten, 31773
- Rekruttering
- Periodontology Clinic at Faculty of Dentistry Tanta University
-
Kontakt:
- rehab f ghouraba, PHD
- Telefonnummer: +201211512429
- E-mail: rehab_ghouraba@dent.tanta.edu.eg
-
Kontakt:
- Aliaa S Kishk, Batchelor
- Telefonnummer: +201015101949
- E-mail: Aliaa8271staff@dent.tanta.edu.eg
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria:
- Patients in good health with absence of any relevant medical condition that contraindicates dental implant placement e.g. blood coagulation disorder.
- Optimal compliance is evidenced by no missed treatment appointments and a positive attitude toward oral hygiene.
- Extraction socket type I according to Ellian et al criteria with adequate native/apical bone to achieve primary implant stability and intact buccal plate of bone.
- Thick mucosal phenotype.
- Probing depth ≤ 3 mm at mid-buccal aspect of failing tooth.
- Age ranged from 18- 35 years old of both genders.
Exclusion Criteria:
- Patients subjected to irradiation in the head and neck area.
- Bisphosphonate therapy.
- Females who are pregnant or trying to conceive, and nursing mothers.
- Smokers and uncontrolled diabetic patients.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: SocketFit Static Surgical Guide
Participants will undergo immediate implant placement in the anterior esthetic zone using the SocketFit static surgical guide.
The guide incorporates a socket-engaging extension designed to enhance guide stability and drilling accuracy following atraumatic tooth extraction.
Implant placement will be performed according to the planned digital workflow.
|
Participants will undergo immediate implant placement in the anterior esthetic zone using the SocketFit static surgical guide.
The guide incorporates a socket-engaging extension designed to enhance guide stability and drilling accuracy following atraumatic tooth extraction.
Implant placement will be performed according to the planned digital workflow.
|
|
Aktiv komparator: Conventional Static Surgical Guide
Participants allocated to the control group will undergo immediate implant placement in the anterior esthetic zone using a conventional tooth-supported static surgical guide designed through the standard digital workflow.
Following atraumatic tooth extraction, the guide will be seated on the remaining teeth to direct sequential osteotomy preparation and implant placement according to the preoperative virtual implant plan.
All other surgical procedures, implant system, drilling protocol, and postoperative management will be identical to those used in the experimental group.
|
Participants allocated to the control group will undergo immediate implant placement in the anterior esthetic zone using a conventional tooth-supported static surgical guide designed through the standard digital workflow.
Following atraumatic tooth extraction, the guide will be seated on the remaining teeth to direct sequential osteotomy preparation and implant placement according to the preoperative virtual implant plan.
All other surgical procedures, implant system, drilling protocol, and postoperative management will be identical to those used in the experimental group.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Coronal deviation
Tidsramme: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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The linear distance (mm) between the planned and actual implant positions at the coronal platform, measured by digital superimposition of the preoperative implant plan and postoperative Cone Beam Computed Tomography (CBCT) data.
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Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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apical deviation
Tidsramme: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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The linear distance (mm) between the planned and actual implant positions at the implant apex, measured using digital superimposition of the preoperative implant plan and postoperative Cone Beam Computed Tomography (CBCT) data.
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Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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depth(vertical) deviation
Tidsramme: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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The vertical difference (mm) between the planned and actual implant positions along the implant long axis, measured using digital superimposition of the preoperative implant plan and postoperative Cone Beam Computed Tomography (CBCT) data.
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Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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angular deviation
Tidsramme: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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The angular difference (degrees) between the long axes of the planned and actual implant positions, measured using digital superimposition of the preoperative implant plan and postoperative Cone Beam Computed Tomography (CBCT) data.
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Immediately after implant placement following digital superimposition of the planned and actual implant positions.
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Aliaa s. Kishk, Batchelor, Tanta University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. august 2026
Primær færdiggørelse (Anslået)
1. juli 2027
Studieafslutning (Anslået)
1. juli 2027
Datoer for studieregistrering
Først indsendt
7. august 2026
Først indsendt, der opfyldte QC-kriterier
7. august 2026
Først opslået (Faktiske)
12. august 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
13. august 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
11. august 2026
Sidst verificeret
1. august 2026
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 3626
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
IPD-planbeskrivelse
No individual participant data (IPD) will be shared.
All personal identifiers, including names and any information that could identify participants, will be removed before data analysis or sharing.
De-identified Cone Beam Computed Tomography (CBCT) images, Stereolithography (STL ) models, and summary outcome data may be used in scientific publications or presentations in accordance with participant consent, ethical approval, and institutional regulations.
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