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Clinical Trials/NCT05878392
NCT05878392CompletedNot Applicable

Comparison Between Different Filling Materials in Immediate Implant

Mansoura University2 sites in 1 country36 target enrollmentStarted: January 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
36
Locations
2
Primary Endpoint
marginal bone loss

Study Overview

Brief Summary

36 patients, were included in this study. They were chosen from the Outpatient Clinic in the Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University for replacement of non-restorable maxillary anterior and premolar teeth (esthetic zone) by immediate implant.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

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

Inclusion Criteria

  • Patient medically free from systemic diseases.
  • Age above 18 years.
  • A single maxillary anterior or premolar tooth that cannot be restored.
  • No acute infection is present.
  • Patients with sufficient quality and quantity of bone.
  • Free from history of bruxism.

Exclusion Criteria

  • A medical condition that would prevent implant surgery.
  • Existence of non-treated generalized progressive periodontitis.
  • Patients who are smokers.

Outcomes

Primary Outcomes

marginal bone loss

Time Frame: 1 year

Cone Beam CT (CBCT) was used measure marginal bone loss

Secondary Outcomes

  • Implant Stability:(1 year)
  • Peri-implant Pocket depth(1 year)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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