MedTrace Logo

Peri-implant Tissues in BLX® Implants

NCT03720236 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2020-07-07

No results posted yet for this study

Summary

This is a randomized triple-blind clinical trial to evaluate the behavior of peri-implant tissues (bone and soft tissues) in BLX implants loaded early or delayed and with different surgical milling protocols. To this end, 40 BLX implants with a diameter of 3.75x10 will be placed in areas of mature bone scarred after extraction. They will be divided into 2 study groups, and these in turn into two subgroups. Group A: complete milling, Group B: partial milling. Each group will be assigned with code 1: early load and code 2: deferred load. Clinical and radiological parameters will be evaluated.

Conditions

  • Dental Implant Failed
  • Dental Prosthesis Failure

Interventions

PROCEDURE

Implant bed preparation protocol

This is the first surgical phase, we prepare the implant bed by using different increasing size drills.

PROCEDURE

Implant loading

This is the second phase, based on prosthetic procedures, to design the crown over the dental implant

Sponsors & Collaborators

  • Manohay Dental SAU

    collaborator UNKNOWN

  • University of Santiago de Compostela

    lead OTHER

Principal Investigators

  • Mario Perez Sayans, PhD · University of Santiago de Compostela

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-11-02
Primary Completion
2019-01-10
Completion
2020-06-19

Countries

  • Spain

Study Locations

More Related Trials

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 NCT03720236 on ClinicalTrials.gov