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Immediate Vs. Early Loading of Immediately Placed Implants

NCT05869292 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2023-05-22

No results posted yet for this study

Summary

The study aims to compare implant stabilities between immediate and early loaded, immediately placed bone-level tapered dental implants in the upper jaw in the partial and total edentulous patients assessing marginal bone loss, oral health-related quality of life, and patient satisfaction within one, two and five years of follow-ups.

Conditions

  • Implant Complication
  • Implant

Interventions

DEVICE

Immediate implant loading

Implants will be received immediately prosthetic restoration following surgical procedure. For the provisional restoration, an open tray impression technique will be used. Plaster models with scan bodies will be digitized by the laboratory scanner (3Shape E1, 3Shape, Kopenhagen, Denmark), and the virtual design of provisional restoration will be performed with 3D designing software (Exocad-Matera 2.3, Exocad, Darmstadt, Germany). Provisional restorations will be then created using polymethyl methacrylate (PMMA) (Telio®CAD, Ivoclar Vivadent, Schaan, Lichtenstein) and were drilled from PMMA blocks using the 5-axis milling machine (Zenotec Select, Wieland, Pforzheim, Germany). Screw-retained abutments for the prosthetic bridge will be chosen according to implant angulation and surrounding soft tissue height. At the end of the six-week healing period, definitive prosthetic restorations will be manufactured and delivered to the patients.

DEVICE

Early implant loading

Implants won't receive immediately prosthetic restoration following surgical procedure and will be left only healing caps. At the end of the six-week healing period, definitive prosthetic restorations will be manufactured and delivered to the patients.

Sponsors & Collaborators

  • University of Belgrade

    lead OTHER

Principal Investigators

  • Aleksa Markovic, Professor · School of Dental Medicine, University of Belgrade

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2019-01-31
Primary Completion
2021-05-15
Completion
2023-05-01

Countries

  • Serbia

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 NCT05869292 on ClinicalTrials.gov