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The Vestibular Socket Therapy : A Novel Concept for Immediate Implant Placement in Defective Fresh Extraction Sites

The Vestibular Socket Therapy : A Novel Concept for Immediate Implant Placement in Defective Fresh Extraction Sites

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03987646
Enrollment
12
Registered
2019-06-17
Start date
2018-05-24
Completion date
2019-08-08
Last updated
2019-09-25

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

Conditions

Immediate Implants

Keywords

xenograft cortical flexible sheet, fresh extraction socket

Brief summary

This article aims to provide a non- staged treatment protocol to placing dental implants in compromised fresh sockets in the aesthetic zone.

Detailed description

This is a site-specific therapy uses study a slowly resorbing regenerative barrier (shield) to augment any thin or deficient labial plate of bone, enhances the overlying soft tissue quality and quantity at the same time with implant fixture placement using a computer-guided surgical template.

Interventions

PROCEDURENon-staged vestibular fresh socket therapy

a slowly resorbable membrane shield is placed above the labial plate of bone so that when the thin labial plate started its resorption process the shield remains till a complete gap fill occurred thus leading to a thicker labial plate of bone or it preserves the socket architecture until a complete bone fill occurred inside the socket

Sponsors

Alexandria University
CollaboratorOTHER
Nourhan M.Aly
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* A hopeless single tooth in the maxillary anterior region * Sufficient apical bone to allow adequate anchorage/primary stability of the implant * had natural teeth present adjacent to the tooth being replaced

Exclusion criteria

* Presence of acute infection * Impossibility of reaching adequate implant primary stability in the native * Smokers of \> 10 cigarettes * Antitumor chemotherapy or radiotherapy in the previous year

Design outcomes

Primary

MeasureTime frameDescription
radiographic buccal bone thickness6 monthspreoperative and follow up CBCTs are superimposed on each other and buccal bone thickness is measure at 3 similar points on both CBCTs and then a mean is calculated
radiographic buccal bone height6 monthspreoperative and follow up CBCTs are superimposed on each other and buccal bone height is measured in relation to implant shoulder level

Secondary

MeasureTime frameDescription
final esthetic outcome of soft tissue6 monthsPink esthetic score. based on subjective assessment of mesial papilla, distal papilla, midfacial level, midfacial contour, alveolar process deficiency, soft tissue color and texture. each item is given a score between 0 and 2, where 0 is the worst and 2 is the best outcome. Then, a final score ranging between 0-14 is calculated

Countries

Egypt

Outcome results

None listed

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