Comparison of Different Materials Contribution to Implants Stability

NCT03501199 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2019-03-05

No results posted yet for this study

Summary

The investigators will use two types of material(PRF-Xenograft) in the buccal gap after immediate dental implant placement. The study design has three groups PRF, graft, and control group. The patients will randomly be assigned to groups by envelop method. The resonance frequency analysis device(Osstell) will be used to measure primary and secondary stabilization. Then the investigators will evaluate each materials' contribution to stability.

Pre-op and 9th month Post-op CBCTs will evaluate about bone loss in mesial-distal and horizontal dimensions.

Conditions

  • Dental Implant Failure Nos

Interventions

OTHER

platelet-rich fibrin placement

filling the buccal gap with platelet-rich fibrin after immediate dental implant placement

OTHER

xenogenic graft placement

filling the buccal gap with xenogenic graft after immediate dental implant placement

OTHER

no extra material

filling the buccal gap with no material after immediate dental implant placement

PROCEDURE

tooth extraction

extraction of tooth which is unrestorable

PROCEDURE

immediate implant placement

putting dental implant into a socket which has been prepared with compatible drills

OTHER

collagen membran placement

placing collagen membran on extraction socket after dental implant placement to cover all

PROCEDURE

raising flap

raising the buccal flap with two vertical incision to cover extraction socket for primary closure

Sponsors & Collaborators

  • Necmettin Erbakan University

    lead OTHER

Principal Investigators

  • Alparslan Esen · Consultant

  • Gökhan Gürses · Care Provider

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-03-01
Primary Completion
2018-05-31
Completion
2019-03-04

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03501199 on ClinicalTrials.gov