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Clinical Trials/NCT06254378
NCT06254378
Not Yet Recruiting
N/A

Evaluation of the Efficacy of Allograft Versus Tenting Technique in Open Sinus Lifting With Immediate Implant Placement A Randomized Clinical Trial

Cairo University0 sites20 target enrollmentMarch 1, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Sinus; Dental
Sponsor
Cairo University
Enrollment
20
Primary Endpoint
Implant stability
Status
Not Yet Recruiting
Last Updated
2 years ago

Overview

Brief Summary

Implant placement in deficient posterior maxilla is a challenging clinical situation that necessitates appropriate treatment options to restore this area.

-Aim of the study: To compare allograft vs tenting technique in terms of implant stability and bone height.

Detailed Description

Rationale for carrying out the trial: The research population will be divided into two groups. Group1 will be treated by allograft with immediate implant technique, Group2 will be treated by tenting technique with immediate implant technique. Allograft has been effective in augmenting bone growth and has been proven to be a vital asset in sinus lifting.

Registry
clinicaltrials.gov
Start Date
March 1, 2024
End Date
October 30, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amira Raafat Ahmed Elshikh

Dentist

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patient with missing upper pre molar , molar teeth
  • Patients in need of bone grafting of the maxillary sinus to house an implant.
  • Patients with residual alveolar crest of at least 3-4mm in height and 5mm in width distal to the canine as measured on CBCT scan
  • Patients with adequate inter-arch space

Exclusion Criteria

  • Patients suffering from any sinus pathosis.
  • Patients who are heavy smokers (\>10 cigarettes/day).
  • Patient under psychiatric therapy or unrealistic expectations
  • Patients of systemic conditions that may interfere with carrying out the surgical procedure.
  • Lack of opposite occluding dentition/prosthesis in the area intended for implant placement
  • Severe bruxism or clenching
  • Poor oral hygiene (full mouth bleeding on probing and full mouth plaque index \>25%)

Outcomes

Primary Outcomes

Implant stability

Time Frame: During the implant placement procedure and after 6 months

implant stability quotient(ISQ) is the evaluation unit set to determine the correct isq\<60:low stability isq 60-65 : medium stability isq \>70: high stability stability of the implant, this module by means of a resonance frequency analysis (rfa) applied to the bone manages to measure stability on an isq scale from 1 to 100 (khz):

Secondary Outcomes

  • Bone hight(Before surgery and after 6 months)

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