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Enrolling by invitationNCT06881095socket shieldUpdated Mar 18, 2025

Immediate Dental Implant Installation With and Without Socket Shield Technique in Aesthetic Zone

An interventional study of socket shield technique group (study group) and conventional immediate implant without socket shield technique in Immediate Dental Implants, Thin Labial Plate of Bone Pre-extraction and Hopeless Tooth in Esthetic Zone, sponsored by Tanta University. Enrolling by invitation at 1 site in Egypt. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-03-18.

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

From the registry’s dates

  • Primary completion was expected by May 2025, 1 year 4 months ago, but the record still lists the study as enrolling by invitation.
  • Registered 11 months after the study started (first participant enrolled Mar 2024, registered Mar 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

20 patients with non-restorable anterior teeth underwent extraction with immediate implant installation using either the immediate implant with socket shield technique or the conventional immediate dental implant.

the socket shield technique group (study group): 10 patients will have immediate implant placement with the socket shield technique.

  • conventional immediate dental implant technique (control group): 10 patients will have immediate implant placement with conventional technique.
Read the detailed description

20 patients with non-restorable anterior teeth underwent extraction with immediate implant installation randomized to two groups immediate dental implant with the socket shield technique group (study group): 10 patients will have immediate implant placement with socket shield technique.

  • conventional immediate dental implant technique (control group): 10 patients will have immediate implant placement with conventional technique without socket shield technique.

preparation of shield: the root will be sectioned in a mesio-distal direction along its long axis, sectioning divided the tooth root into one facial third and two palatal thirds, Periotomes will then be inserted between the palatal root section and the alveolar socket wall to sever the PDL and this section of root was then carefully delivered so as not to disturb the facial root section, the remaining root section was then reduced coronally to 1 mm above the alveolar crest.

The tooth socket's palatal wall and apex will be then curetted to remove any tissue or infective remnants and the root section was checked for immobility with a sharp probe.

After completion of the previous steps, the tooth root here will be known as the socket- shield (SS). An osteotomy was then sequentially prepared according to manufacturer instructions and a suitable implant then inserted palatal to the SS.

02

Conditions studied

  • Immediate Dental Implants
  • Thin Labial Plate of Bone Pre-extraction
  • Hopeless Tooth in Esthetic Zone

Keywords

  • socket shield technique
  • partial extraction therapy
  • immediate dental implant
03

In context

Lead sponsor

Tanta University is the lead sponsor of 963 studies on the registry; 304 are open to participants now.

Of its 16 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 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

    1. Non restorable maxillary anterior teeth without periapical pathology that may affect the success of dental implants.
  1. Interarch space enough for prosthetic rehabilitation. 3. Presence of posterior teeth or prosthesis that maintain occlusal bite. 4. Adult patients. 5. Good oral hygiene.

Exclusion criteria

Exclusion Criteria:

    1. Edentulous anterior maxillary region. 2. Bad oral hygiene. 3. Patients with any relevant systemic diseases that affect soft tissue or bone healing.
  1. Patients with parafunctional habits (bruxism and clenching). 5. Uncooperative patients. 6. Heavy smokers.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    socket shield technique group (study group)

    the socket shield technique group (study group): 10 patients will have immediate implant placement with socket shield technique. * conventional immediate dental implant technique (control group): 10 patients will have immediate implant placement with conventional technique without socket shield technique. preparation of shield: the root will be sectioned in a mesio-distal direction along its long axis, sectioning divided the tooth root into one facial third and two palatal thirds, Periotomes will then be inserted between the palatal root section and the alveolar socket wall to sever the PDL and this section of root was then carefully delivered so as not to disturb the facial root section, the remaining root section was then reduced coronally to 1 mm above the alveolar crest. The tooth socket's palatal wall and apex will be then curetted to remove any tissue or infective remnants and the root section was checked for immobility with a sharp probe. After completion of th

    Procedure: socket shield technique group (study group)

  • Experimental
    conventional immediate implant without socket shield technique(control group)

    conventional immediate implant without socket shield technique: • After administration of local anesthesia, atraumatic tooth extraction by extraction forceps and Periotomes, an osteotomy was then sequentially prepared according to manufacturer instructions and a suitable implant then inserted and placement of cover screw. However, the soft tissue contour formed after healing may need some modification prior to impression taking. Suturing around the healing abutment, suture will be removed one week post surgically and then healing abutment and final prosthetic loading will be done after 4-6 months.

    Procedure: conventional immediate implant without socket shield technique

Interventions

  • Proceduresocket shield technique group (study group)

    immediate implant installation with socket shield technique: After administration of local anesthesia, the root will be sectioned in a mesio-distal direction along its long axis, sectioning divided the tooth root into one facial third and two palatal thirds. Periotomes will then be inserted between the palatal root section and the alveolar socket wall to sever the PDL and this section of root was then carefully delivered so as not to disturb the facial root section, the remaining root section was then reduced coronally to 1 mm above the alveolar crest. The tooth socket's palatal wall and apex will be then curetted to remove any tissue or infective remnants, and the root section was checked for immobility with a sharp probe. After completion of the previous steps, the tooth root here will be known as the socket- shield (SS). An osteotomy was then sequentially prepared according to manufacturer

    Also known as: partial extraction therapy

  • Procedureconventional immediate implant without socket shield technique

    • After administration of local anesthesia, atraumatic tooth extraction by extraction forceps and Periotomes, an osteotomy was then sequentially prepared according to manufacturer instructions and a suitable implant then inserted and placement of cover screw. However, the soft tissue contour formed after healing may need some modification prior to impression taking. Suturing around the healing abutment, suture will be removed one week post surgically and then healing abutment and final prosthetic loading will be done after 4-6 months.

06

What researchers measure

Primary outcomes

  1. labial bone thickness

    1. labial bone thickness measuring thickness of labial bone labial to the implant by (CBCT) Cone beam computed tomography

    Time frame: 6 months

  2. marginal bone loss

    Time frame: 6 months

Secondary outcomes

  1. bone density around dental implant

    bone density around dental implant by Cone beam computed tomography

    Time frame: 6 months

  2. implant secondary stability

    Secondary implant stability: will be recorded just after uncovery using Resonance frequency analysis (RFA) device \* (Osstell).

    Time frame: 6 months

  3. implant success

    absence of infection, fistula formation or implant mobility

    Time frame: 6 months

07

Study locations

1 site
  • Faculty of Dentistry
    Tanta, 3111, Egypt
08

References and documents

Individual participant data

Plan to share: No

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 Mar 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06881095
Lead sponsor
Tanta University
Responsible party
Islam Ahmed Elsayed (master degree( Principal Investigator), Tanta University) — Principal investigator
First posted
Mar 18, 2025
Start date
Mar 25, 2024
Primary completion
May 12, 2025 (estimated)
Completion
Jun 16, 2025 (estimated)
Last update
Mar 18, 2025

Study contacts

islam ahmed abo elela, master study
principal investigator · faculty of dentistry tanta university
Ibrahim mohammed nowair, professor
principal investigator · faculty of dentistry tanta university
Rafic ramadan bedir, professor
principal investigator · faculty of dentistry tanta university
Wesam Hamed Elsaadany, lecturer
principal investigator · faculty of dentistry tanta university

Oversight

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

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