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Clinical Trials/NCT04905758
NCT04905758CompletedNot Applicable

Soft and Hard Tissues Evaluation Around Immediately Placed New Implant Design: Randomised Clinical Study

Kafrelsheikh University2 sites in 1 country50 target enrollmentStarted: April 1, 2020Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
50
Locations
2
Primary Endpoint
marginal bone level
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

patients were randomly divided into Maxi-Z plus dental implant group versus Maxi-Z implant group

Detailed Description

after tooth extraction implants will be placed immediately and provisional restoration will be placed in both groups to detect the advantaged and drawbacks of newly designed Maxi-Z plus dental implant versus Maxi-Z dental implant

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

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

Inclusion Criteria

  • •good health
  • •unrestorable, periodontal healthy teeth

Exclusion Criteria

  • •systemic disease
  • •periodontal disease
  • •presence of abscess

Outcomes

Primary Outcomes

marginal bone level

Time Frame: 12 months

measured in mm using X-ray

Implant mobility using Periotest M

Time Frame: 12 months

Periotest M values range from (-8 to 0). high values represent loose implant, while osseointegrated implants showed low values

Secondary Outcomes

  • pink estheic score(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Walid Elamrousy

lecturer of oral medicine and periodontology

Kafrelsheikh University

Study Sites (2)

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