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Search / Trial NCT05106855

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

Launched by UNIVERSITY OF SANTIAGO DE COMPOSTELA · Oct 29, 2021

Trial Information

Current as of July 04, 2025

Recruiting

Keywords

Immediate Implant Post Extraction Implant Early Loading Photobiomodulation Oral Rehabilitation

ClinConnect Summary

This clinical trial is studying a new approach to placing dental implants immediately after a tooth is extracted. The goal is to see how well these implants work in terms of stability and bone health when compared to traditional methods. Some participants will receive implants with a special low-level laser treatment, while others will not. This trial aims to find out if the laser treatment helps improve the outcomes for patients who need dental implants.

To participate in this study, candidates must be adults aged 65 to 74 with at least one tooth that needs to be removed. They should not have any infections in the implant area, significant medical issues, or be heavy smokers. Participants can expect to have their dental implants placed soon after tooth extraction and will be monitored for how well the implants integrate into the bone and how much bone loss occurs around them. It's important to know that patients will need to give their consent to participate and will be informed about the study thoroughly.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients satisfying all inclusion criteria and none of the exclusion criteria will be informed verbally and in writing about the study and signed the informed consent form.
  • The implant area is free of infection
  • Patients without systemic pathology or medical and general contraindications that are absolute contraindications for surgical procedures;
  • Adults who agree to take part in the study and signed the informed consent form.
  • Smokers of less than 5 cigarettes/day.
  • Not to be completely edentulous.
  • Need for extraction of at least one tooth.
  • Post-extraction bone area (fresh alveolus).
  • Patients with sufficient bone height to obtain primary stability for implant installation (2 mm longer than the largest root).
  • Edentulous areas with sufficient mesial-distal, buccolingual and interocclusal space for the placement of an anatomical restoration with a prosthetic space of at least 5 mm.
  • Exclusion Criteria:
  • Immunosuppressed.
  • Smokers of more than 5 cigarettes/day.
  • Bleeding rate greater than 30 %.
  • Presence of active or uncontrolled periodontal disease;
  • Patients with less than 2 mm of keratinised gingiva.
  • Implants with primary stability with ISQ \< 50
  • When this is not possible, assume a security margin to the inferior dental nerve of at least 1 mm.
  • Previus history of local radiotherapy in the head and neck region.

About University Of Santiago De Compostela

The University of Santiago de Compostela, a prestigious institution located in Spain, is dedicated to advancing scientific research and healthcare through innovative clinical trials. With a rich history of academic excellence, the university fosters a multidisciplinary approach, bringing together experts in medicine, pharmacology, and public health to conduct rigorous studies aimed at improving patient outcomes. Committed to ethical practices and the highest standards of research integrity, the university collaborates with various stakeholders, including healthcare providers and industry partners, to translate findings into real-world applications that enhance medical knowledge and treatment options.

Locations

Santiago De Compostela, A Coruña, Spain

Santiago De Compostela, , Spain

Patients applied

AG

1 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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