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Clinical Trials/NCT05670067
NCT05670067
Completed
Not Applicable

Localized Alveolar Ridge Reconstruction and Soft Tissue Augmentation Using a Triple Graft From the Maxillary Tuberosity Simultaneous With Immediate Implant Placement ( a Randomized Clinical Clinical Study)

Ain Shams University1 site in 1 country24 target enrollmentOctober 30, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Immediate Implant Placement
Sponsor
Ain Shams University
Enrollment
24
Locations
1
Primary Endpoint
buccal bone thickness
Status
Completed
Last Updated
last year

Overview

Brief Summary

In the study immediate implant is placed in the anterior region with autogenous bone grafting from the maxillary tuberosity in one group and in the other group immediate implant is placed with xenograft .IN both groups soft tissue grafting is done using connective tissue assessment of buccal bone thickness and soft tissue will be done 6 months post operative

Detailed Description

immediate implant will be placed in the anterior region with autogenous graft from the maxillary tuberosity and in the other group immediate implant will be laced with xenograft soft tissue grafting using sub-epithelial connective tissue will in both groups assessment of buccal bone thickness is the primary outcome of the study, while volumetric assessment of the soft tissue and patient satisfaction are the secondary and tertiary outcome the assessment of all outcome will be 6 months post operative the extraction socket in which the implant will be placed are class I\&II

Registry
clinicaltrials.gov
Start Date
October 30, 2021
End Date
January 5, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed Hesham Mohamed

assistant lecturer

Ain Shams University

Eligibility Criteria

Inclusion Criteria

  • Systemically healthy patients (American Society of Anesthesiologists I; ASA I).
  • Age range (20-40) years.
  • Good compliance with the plaque control instructions following initial therapy.
  • Patients diagnosed with bone defect in the maxillary anterior esthetic zone (class 1 \& 2)
  • Availability for follow up and maintenance program.

Exclusion Criteria

  • Peri apically infected teeth
  • Presence of smoking habit.
  • Presence of occlusal interferences.
  • Pregnant females.
  • Vulnerable group of patients (handicapped, mentally retarded and prisoners) (according to the recommendation of esthetical committee of Faculty of Dentistry Ain Shams University).

Outcomes

Primary Outcomes

buccal bone thickness

Time Frame: at baseline and 9 months

measuring the buccal bone thickness using CBCT

Secondary Outcomes

  • soft tissue assessment using pink esthetic score(9 months post opertive)
  • patient satisfaction(after 9 months)

Study Sites (1)

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