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Single Tooth Restoration in the Maxilla Using the Straumann® PURE® Ceramic Implant Monotype: One Year Follow up

NCT03352284 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2021-07-22

No results posted yet for this study

Summary

The main objective is to evaluate peri-implant hard and soft tissues's stability with the use of a ceramic implant (Implant Straumann®Pure Ceramic) during one year follow up.

Conditions

  • Ceramic Implant

Interventions

DEVICE

Straumann Pure Ceramic Implant

The surgical technique begins with the lift of a vestibular mucoperiosteal flap respecting the papillae of the adjacent teeth. After the alveolar bone is exposed, the sequence of drilling and placement of the intra-bone fixation are carried out. In case of fenestrations or dehiscence, they are treated by xenograft and collagen-absorbable membrane. Once the implant is placed, a healing cap or provisional prosthesis is placed depending on the torque achieved. Finally, the flap is replaced and sutured.

Sponsors & Collaborators

  • Miren Vilor Fernández

    lead OTHER

Principal Investigators

  • Luis Antonio Aguirre Zorzano, Dr. · University of the Basque Country (UPV/EHU)

  • Luis Barbier Herrero, Dr. · University of the Basque Country (UPV/EHU)

  • Miren Vilor Fernández, Lcda. · University of the Basque Country (UPV/EHU)

  • Ana Maria García de la Fuente, Dr. · University of the Basque Country (UPV/EHU)

  • Ruth Estefanía Fresco, Dr. · University of the Basque Country (UPV/EHU)

  • Xabier Marichalar Mendia, Dr. · University of the Basque Country (UPV/EHU)

  • Elena Ruiz de Gopegui Palacios, Lcda. · University of the Basque Country (UPV/EHU)

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2014-05-01
Primary Completion
2019-12-31
Completion
2020-12-31

Countries

  • Spain

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 NCT03352284 on ClinicalTrials.gov