ClinConnect ClinConnect Logo
Search / Trial NCT01836744

Survival Rate of Dental Implants Placed in Sinus Lift Performed With Two Different Grafts

Launched by GRUPO DE INVESTIGAÇÃO: CIRURGIA ORAL, PERIDONTOLOGIA, IMPLANTOLOGIA · Apr 17, 2013

Trial Information

Current as of May 27, 2025

Completed

Keywords

ClinConnect Summary

The study will be performance in 12 patients submitted to a bilateral sinus lift procedure.

Six months after the bilateral sinus lifting performed in a randomly way, using as graft materials (100% of autologous bone graft or 100% of xenograft), will be placed 1 to 3 implants in each maxillary sinus.

Wait more six months to expose the implant. At the end of 13 months after implant placement it should be in charge.

Implant placement (6 months after sinus lift procedure):

* Both sides should be treated during the same session.
* Patients will receive 2g Amoxicillin one hour before the proc...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Any partially edentulous patient having bilateral edentulism in the posterior maxillae (premolars and/or molars) with a similar degree of bone resorption requiring one to three implants at each side, being 18 years or older, and able to sign an informed consent. For all the potentially included patients preoperative CBCT (cone beam computed tomography) or CT scans and OPGs (orthopantomograph)must be obtained and attached to the files. The vertical bone height below the maxillary sinus at the implant sites must be of 1-5 mm and bone thickness at least 6 mm measured on CBCT (cone-beam computed tomography)or CT scans. Smokers will be included and patients will be grouped into: 1) non smokers; 2) light smokers ≤ 10 cigarettes/day; 3) heavy smokers ≥ 11 cigarettes/day, according to what they declare.
  • Exclusion Criteria:
  • General contraindications to implant surgery.
  • Patients irradiated in the head and neck area.
  • Immunosuppressed or immunocompromised patients.
  • Patients treated or under treatment with intravenous amino-bisphosphonates.
  • Patients with untreated periodontitis.
  • Patients with poor oral hygiene and motivation.
  • Uncontrolled diabetes.
  • Pregnancy or nursing.
  • Substance abuser.
  • Psychiatric problems or unrealistic expectations.
  • Lack of opposite occluding dentition in the area intended for implant placement.
  • Patients with an acute or chronic sinusitis.
  • Patients participating in other trials, if the present protocol cannot be properly adhered too.
  • Patients referred only for implant placement.
  • Patient unable to be followed for 5 years after loading.

About Grupo De Investigação: Cirurgia Oral, Peridontologia, Implantologia

The research group specializes in oral surgery, periodontology, and implantology, focusing on advancing clinical practices and enhancing patient outcomes through rigorous scientific investigation. Comprising a multidisciplinary team of experts, the group is dedicated to exploring innovative techniques and therapies within the dental field, aiming to address critical challenges in oral health. By conducting well-designed clinical trials, they seek to contribute valuable insights to the literature and improve standards of care in dentistry.

Locations

Oporto, Porto, Portugal

Patients applied

0 patients applied

Trial Officials

Francisco Correia, DDS, Msc, PhD

Principal Investigator

Universidade do Porto

Ricardo Faria Almeida, DDS, Msc, PhD

Study Director

Universidade do Porto

Antonio Campos Felino, DDS, PhD

Study Chair

Universidade do Porto

Sonia Gouveia, Phd

Study Chair

Instituto de Engenharia Eletrónica e Informática de Aveiro (IEETA/UA) and Centro de I&D em Matemática e Aplicações (CIDMA/UA), Universidade de Aveiro (UA), Portugal

Daniel H Pozza, DDS, PhD

Study Chair

Departamento de Biomedicina da Faculdade de Medicina, and Faculdade de Ciências da Nutrição e Alimentação, and I3s, Universidade do Porto, Porto, Portugal.

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials