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Survival Rate of Dental Implants Placed in Sinus Lift Performed With Two Different Grafts

NCT01836744 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2023-09-13

No results posted yet for this study

Summary

Previous in a randomized way, it will be performance 12 bilateral sinus lift with autologous bone in one side and the in other with xenograft material. After 6 mouths we will place 1 to 3 implants in each side and analyse the survival rate and possibles differences related to; prosthesis failure; biological and prosthetic complications; peri-implant marginal bone level changes.

Conditions

  • Dental Implant Survival Rate

Interventions

DEVICE

Survival rate dental implant (OsseoSpeed™)

Sponsors & Collaborators

  • Universidade do Porto

    collaborator OTHER

  • Dentsply Sirona Implants and Consumables

    collaborator INDUSTRY

  • Tecnoss OsteoBiol

    collaborator UNKNOWN

  • Grupo de Investigação: Cirurgia Oral, Peridontologia, Implantologia

    lead OTHER

Principal Investigators

  • Francisco Correia, DDS, Msc, PhD · Universidade do Porto

  • Ricardo Faria Almeida, DDS, Msc, PhD · Universidade do Porto

  • Antonio Campos Felino, DDS, PhD · Universidade do Porto

  • Sonia Gouveia, Phd · Instituto de Engenharia Eletrónica e Informática de Aveiro (IEETA/UA) and Centro de I&D em Matemática e Aplicações (CIDMA/UA), Universidade de Aveiro (UA), Portugal

  • Daniel H Pozza, DDS, PhD · Departamento de Biomedicina da Faculdade de Medicina, and Faculdade de Ciências da Nutrição e Alimentação, and I3s, Universidade do Porto, Porto, Portugal.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-03-18
Primary Completion
2017-06-20
Completion
2023-07-30

Countries

  • Portugal

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 NCT01836744 on ClinicalTrials.gov