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Clinical Trials/NCT06515509
NCT06515509CompletedNot Applicable

Evaluation of the Dimensional Alveolar Bone Changes in Immediate Post Extraction Implant Placement in the Maxillary Premolar Area With or Without Loading: A Randomized Controlled Clinical Trial

Cairo University1 site in 1 country30 target enrollmentStarted: July 16, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Height of alveolar bone crest

Study Overview

Brief Summary

The aim of this study was to evaluate the dimensional alveolar bone changes in immediate post extraction implant placement with loading compared to immediate post extraction implant placement without loading in the maxillary premolar area . The main question it aims to answer is : Can immediate post extraction implant placement in the maxillary premolar area with loading achieve better alveolar bone dimensions than without loading?

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
25 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •1. Patients who have at least one non restorable tooth in the maxillary premolar area that needs to be extracted.
  • •2. Patients with healthy systemic condition.
  • •Patients aged from 20 to 45 years old.
  • •Buccal bone thickness should be at least 1mm. (Morton et al., 2014)
  • •Availability of bone apical and palatal to the socket to provide primary stability.(Morton et al., 2014)
  • •Good oral hygiene.(Wiesner et al., 2010)
  • •Accepts one year follow-up period (cooperative patients) Patient provides an informed consent.
  • •8. Adequate Inter-arch space for implant placement.
  • •Favorable occlusion (no traumatic occlusion)

Exclusion Criteria

  • •Patients with signs of acute infection related to the area of interest.
  • •Patients with habits that may jeopardize the implant longevity and affect the results of the study such as parafunctional habits (Lobbezoo et al., 2006).
  • •3. Current and former smokers (Lambert, Morris and Ochi, 2000)
  • •Pregnant females.

Arms & Interventions

Immediate Implants without loading

Active Comparator

Intervention: immediate implant placement with or without loading (Procedure)

Immediate Implants with loading

Active Comparator

Intervention: immediate implant placement with or without loading (Procedure)

Outcomes

Primary Outcomes

Height of alveolar bone crest

Time Frame: 6 months

After the implants are placed, a series of digital radiographs are obtained at 0 , 3, and 6 months duration to study the changes in the amount of crestal bone level.

Secondary Outcomes

  • Implant stability(6 months)
  • post-surgical patient satisfaction(6 months)
  • Alveolar bone width(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Osama Atef Elshahat Attia

Dr. Osama Atef

Cairo University

Study Sites (1)

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