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Clinical Trials/NCT06334081
NCT06334081
Active, not recruiting
Not Applicable

Clinical Outcomes of Two Different Surgical Drilling Protocols of Immediate Loaded Dental Implant in Posterior Maxilla

Mansoura University1 site in 1 country16 target enrollmentJune 29, 2023
ConditionsMissing Teeth

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Missing Teeth
Sponsor
Mansoura University
Enrollment
16
Locations
1
Primary Endpoint
bone density measurement
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

Sixteen dental implants inserted in sixteen patients who were selected from the outpatient clinic of the Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University, for the rehabilitation of missed single maxillary posterior tooth by an immediately loaded dental implants

Detailed Description

16 dental implants were inserted in 16 patients were divided into two groups: Group A: 8 dental implants were inserted using undersized drilling technique and Group B: 8 dental implants were inserted using single drilling technique. then the dental implants were assessed for 6 months regarding Clinical Evalution: regarding these parameters after immediately dental implants loading,3 months and 6 months. implant stability, implant probing depth, bleeding index. Radiographic evaluation: immediately after implant loading and 6 months after loading regarding bone density and marginal bone loss.

Registry
clinicaltrials.gov
Start Date
June 29, 2023
End Date
June 30, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Heba Elsheikh

assistant professor of oral and maxillofacial surgery

Mansoura University

Eligibility Criteria

Inclusion Criteria

  • Patients with missed one or more posterior maxillary tooth.
  • Be older than 18 years and of residual bone height more than10 mm.
  • Patients with good oral hygiene and willing to participate in the follow-up sessions.
  • Patients with adequate mesio-distal width and inter-arch space.
  • Patients without any para-functional habits such as clenching and bruxism.

Exclusion Criteria

  • Patients whose proposed surgical site had any pathological lesion or root tips.
  • Drug or alcohol abuse.
  • Patients with uncontrolled systemic diseases.
  • Pregnant patients.
  • Tobacco use more than fourteen cigarettes daily.

Outcomes

Primary Outcomes

bone density measurement

Time Frame: 6 month

cbct will be done to evaluate difference in bone density

marginal bone loss

Time Frame: 6 month

cbct will be done to evaluate marginal bone loss

Study Sites (1)

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