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Clinical Trials/NCT05005585
NCT05005585
Unknown
Not Applicable

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

Cairo University3 sites in 1 country28 target enrollmentDecember 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Loss of Teeth Due to Extraction
Sponsor
Cairo University
Enrollment
28
Locations
3
Primary Endpoint
Implant survival
Last Updated
4 years ago

Overview

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 .

Registry
clinicaltrials.gov
Start Date
December 1, 2021
End Date
April 1, 2023
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Iman Abd-ElWahab Radi, PhD

Professor of Prosthodontics, Faculty of Dentistry, Cairo University

Cairo University

Eligibility Criteria

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)
  • 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.

Outcomes

Primary Outcomes

Implant survival

Time Frame: 12 months

If 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 Outcomes

  • Changes in the height and thickness of the labial plate of bone(12 months)
  • Changes in soft tissue height(12 months)

Study Sites (3)

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