MedTrace Logo

Lateral Bony Wall Repositioning in Maxillary Sinus Floor Augmentation

NCT04811768 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2021-03-23

No results posted yet for this study

Summary

The aim of the present prospective randomized controlled study is to clinically and histologically investigate the safety and efficacy of bony wall repositioning compared to rotary window preparation with membrane coverage in maxillary sinus floor augmentation.

Conditions

  • Maxillary Sinus Augmentation

Interventions

PROCEDURE

Maxillary sinus augmentation

The surgery was performed under local anaesthesia in both groups, lateral window preparation and window coverage was carried out based on randomization.

Sponsors & Collaborators

  • NSK Europe GmbH

    collaborator INDUSTRY

  • Botiss Medical AG

    collaborator OTHER

  • Institut Straumann AG

    collaborator INDUSTRY

  • Dicomlab Kft.

    collaborator UNKNOWN

  • Hungarian Human Resources Development Operational Program (EFOP-3.6.2-16-2017-00006)

    collaborator UNKNOWN

  • Excellence Program of the Ministry for Innovation and Technology in Hungary

    collaborator UNKNOWN

  • Semmelweis University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2017-03-01
Primary Completion
2018-05-30
Completion
2018-05-30

Countries

  • Hungary

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 NCT04811768 on ClinicalTrials.gov