Skip to content

REPI : a Randomized Open Label Trial Evaluating the Use of APC in Pre-Implantation Reconstruction of Maxilla

Use of Autologous Platelet Concentrate in Pre-Implantation Reconstruction of Maxilla.

Status
Terminated
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00295126
Enrollment
20
Registered
2006-02-22
Start date
2003-05-31
Completion date
2007-11-30
Last updated
2008-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Jaw, Edentulous, Maxillary Diseases, Tooth Loss

Keywords

Edentulous, Tooth Loss, APC, Autologous platelet concentrate

Brief summary

This is a randomized open label trial that evaluates the efficacy of an autologous platelet concentrate (APC) in pre-implantation reconstruction of maxilla. The sinus occlusion will be performed under general anaesthetic. On one side by the usual technique with hipbone transplant, the other side will be restored with APC mixed with autologous bone tissue removed from the surgery site. The side selection will be determined by the randomization.

Detailed description

Rational Maxillary Edentulous is one of the more frequent handicaps that cause many problems for dental prosthesis. Dental implants are currently the most convenient solution but require sufficient bone sinus height. The filling of the sinus can be made by two ways : * Either with autologous bone removed from hipbone or cranial bone. This method has several drawbacks such as the multiplicity of the surgery sites. * Or with alloplasty materials that are subject to uncertain osseointegration and that are very expensive. The aim of this study is to show the interest of an autologous platelet concentrate (APC) in this surgery. We will use the osteogenic property of platelets associated with a small quantity of spongy bone removed from the surgery site. It has been previously demonstrated that platelets contain growth factors, in particular PDGF (platelet derivated growth factors), TGF-α1 and 2 (transforming growth factors) and IGF-1 (insulin like growth factor). These molecules have receptors on spongy bone, enhance mitosis, osteoblast differentiation, angiogenesis and induce the inhibition of osteoclats. Method : The sinus filling will be performed under general anaesthetic. On one side by the usual technique with hipbone transplant, the other side will be restored with APC mixed with autologous bone tissue removed from the surgery site. The side selection will be determined by the randomization. For each patient a waiting period of 6 months is required before dental implants. Twenty patients will be enrolled in this single-centre study with a follow-up of one year. Main objective : \- To demonstrate that the osteogenesis with APC mixed with a small quantity (1 to 2 cm2) of autologous bone tissue removed from the surgery site, has a sufficient quality to allow the dental implants. Secondary Objectives : * To compare the osteogenesis with the current procedure (hipbone transplant) * To estimate the kinetic of osteogenesis using successive radiography.

Interventions

PROCEDUREcellular therapy : Autologous platelet concentrate (APC)

Sponsors

Etablissement Français du Sang
CollaboratorOTHER
University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age above 18 years * ASA1 class of anesthetic risk * SA3 or SA4 of the Misch classification

Exclusion criteria

* Smoker * Progressive sinusal lesion or previous history of maxillary sinusitis * Previous history of maxillary surgery * Hemopathy * Contraindication to cytapheresis * Progressive cardiopathy * Severe cerebellar arteriopathy * Infectious state * Thrombopenia \< 150 g/l controlled by citrate * Serology : antibody anti-HVC, anti-HIV 1 & 2, anti HTLV 1 & 2 positive

Design outcomes

Primary

MeasureTime frame
Radiological outcome measure : the bone height under the sinus on the two sides.

Secondary

MeasureTime frame
Radiological outcome measure : the bone density
Clinical outcome measure : assessment of the alveolar crest quality, possible orals complications, and complications at the removal site.
Histological outcome measures : with bone core boring at the implant site.
All these measurements will be matched for each patient on both sides.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026