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Vestibular Socket Therapy With Simultaneous Implant Placement Versus Contour Augmentation With Early Implant Placement

Vestibular Socket Therapy With Simultaneous Implant Placement Versus Contour Augmentation With Early Implant Placement in Fresh Extraction Sockets : A Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05005585
Enrollment
28
Registered
2021-08-13
Start date
2021-12-01
Completion date
2023-04-01
Last updated
2021-11-18

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

Conditions

Loss of Teeth Due to Extraction

Brief summary

immediate implant placement with VST technique versus early implant placement with contour augmentation in fresh extraction sockets in the esthetic zone.

Detailed description

comparing VST technique with immediate implant placement that end up with final crown after 2 months with contour augmentation with early implant placement after 4- 8 weeks of soft tissue healing , then after 3 months final crown delivery both in fresh extraction sockets in the esthetic zone .

Interventions

PROCEDUREimmediate implant

immediate implant placement with VST technique versus early implant placement with contour augmentation technique

Sponsors

Cairo University
Lead SponsorOTHER

Study design

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

Masking description

outcome assessor isnt involved in the intervension

Intervention model description

VST with immediate implant placement versus contour augmentation with early implant placement in fresh extraction sockets in esthetic zone.

Eligibility

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

Inclusion criteria

Non-restorable maxillary teeth in the esthetic zone Intact adjacent teeth Adequate palatal and apical bone that allows achieving implant primary stability. Compromised sockets type II defect (Nicolas Elian 2007) ≥18 years Systemically healthy patients

Exclusion criteria

Extraction sockets with acute or chronic infection or with adjacent infected teeth Heavy Smokers \> than 10 cigarettes daily Cancer patients undergoing radiotherapy or chemotherapy during or within the last 6 months. Unmotivated patients to maintain adequate oral hygiene to follow up. Patients with physical disabilities that could affect follow up.

Design outcomes

Primary

MeasureTime frameDescription
Implant survival12 monthsIf there is no pain or tenderness on use, no mobility, no history of exudates and radiographic bone loss is less than 2 mm from initial surgery implant the implant is considered successful

Secondary

MeasureTime frameDescription
Changes in the height and thickness of the labial plate of bone12 monthswill be measured by superimposing CBCT images obtained at the baseline (time of tooth extraction) and those after 12 months postimplant placement.
Changes in soft tissue height12 monthswere identified midfacially and at the apex of the mesial and distal papillae by superimposing the STL (Standard Triangle Language) files of the models, obtained via IOS, at the baseline (of the unrestorable tooth) with those after 12 months of implant insertion

Countries

Egypt

Contacts

Primary Contactamir elawady, BDS
amir112093@miuegypt.edu.eg00201020205791
Backup ContactMohamed Elkhashab, PHD
mohamed.elkhashab@dentistry.cu.edu.eg00201006611525

Outcome results

None listed

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