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Comparative Study of Immediate Single Unit Implants in Early Loading Protocols, With or Without Photobiomodulation.

NCT05106855 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2026-02-05

No results posted yet for this study

Summary

Post-extraction implants are an alternative to traditional implant placement on completely healed bone, in order to reduce the number of surgical interventions, shorten treatment time, maintain bone architecture and thus provide better aesthetics. This study focuses on evaluating the results obtained by opting for different immediate placement of single dental implants protocols in a fresh alveolus, and its general objective is to compare implant stability and marginal bone loss (MBL) in implants installed post-extraction. For this, the investigators will placement Grand Morse Acqua or NeoPoros implants (Helix GM - Neodent, Curitiba, Brazil), in early loading protocols, with or without low level laser photobiomodulation (LLLT), in patients attending the Master of Oral Medicine, Oral Surgery and Implantology of the University of Santiago de Compostela for oral rehabilitation using osseointegrated single dental implants in the maxillary and/or mandibular region.

Conditions

  • Dental Implant
  • Tooth Absence
  • Tooth Extraction

Interventions

RADIATION

Low Laser Radiation

One group will receive laser application to check if there is acceleration of healing.

OTHER

Changing the implant surface

Changing the treatment surface of the dental implant to see if osseointegration occurs more quickly.

RADIATION

Low Laser Radiation off

This group will receive laser application off.

PROCEDURE

Implant placement immediately after tooth extraction

When the last alternative is tooth extraction, this will be done, and in the same surgical intervention the dental implant will be placed.

PROCEDURE

Installing the dental crown with early loading

The installation of the dental crowns will be performed in a period of 6 to 8 weeks, after the dental implant has been installed.

Sponsors & Collaborators

  • University of Santiago de Compostela

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-03
Primary Completion
2024-11-30
Completion
2024-12-20

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 NCT05106855 on ClinicalTrials.gov