Who are we?


Signup for

Online registration

Log in to register
your trial

Search a trial




van CCT (UK)

van CCT (UK)

Onderzoek naar kaakbotophoging met kunstbot en stamcellen voor tandwortelimplantaten

- candidate number16379
- NTR NumberNTR4408
- ISRCTNISRCTN no longer applicable
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR7-feb-2014
- Secondary IDsNL29581.000.09 EudraCT 2009-015562-62
- Public TitleOnderzoek naar kaakbotophoging met kunstbot en stamcellen voor tandwortelimplantaten
- Scientific TitleBone augmentation with autologous adipose tissue-derived mesenchymal stem cells and calcium phosphate carriers in the human maxillary sinus floor elevation model
- hypothesisFor patients with maxillary atrophy, the distal area of the maxilla can be augmented by transplanting bone or bone substitutes to the bottom of the maxillary sinus in order to provide sufficient alveolar bone volume for implant placement. The sinus floor elevation (or sinus lift) model is unique since it allows histological examination of biopsies obtained during the preparation for dental implant placement. In this study, the currently used autologous bone grafts and bone substitute materials will be replaced by an osteoinductive implant consisting of a calcium phosphate carrier seeded with clinically relevant quantities of minimally manipulated, freshly isolated adipose tissue stem cells in a one-step surgical procedure. This novel concept can be performed in 2 hours within the surgical theatre using a CE-marked device, thus avoiding costly GMP stem cell expansions and second intervention. We hypothesize that the thus created bioactive implant will lead to faster and improved restoration of maxillary bone volume and functionality without the drawback of complications associated with the currently used implantation materials. If successful, this offers broad potential for other bone tissue engineering applications as well.
- Healt Condition(s) or Problem(s) studiedMesenchymal stem cells, Maxillary sinus, Bone substitute
- Inclusion criteria- minimal bone height of 4 mm at planned implant site(s) - no local need for horizontal bone augmentation - healthy appearance sinus maxillaris - smoking below 10 sigarettes a day
- Exclusion criteria- History of malignancy or chronic infectious disease (i.e. HIV, Hepatitis) - irradiation history in jaw area - destructive sinus surgery indicated during anamnesis - endocarditis or heart valve abnormalities, or heart valve prostheses - abnormalities in the immune system, or use of immune suppressants - severe bone metabolic disorders (e.g. severe osteoporosis treated with bisphosphonates) - Chronic use (>7 consecutive days) of anticoagulants (such as aspirin) or Non-Steroidal Anti-Inflammatory Drugs (NSAIDS) within 15 days prior to lipoaspriation - Signs or symptoms of infection at the time of any surgical procedure - pregnant or nursing, or intention to become pregnant
- mec approval receivedyes
- multicenter trialno
- randomisedyes
- masking/blindingNone
- controlActive
- groupParallel
- TypeSingle arm
- Studytypeintervention
- planned startdate 31-mei-2010
- planned closingdate1-jan-2015
- Target number of participants15
- InterventionsAdipose tissue aspiration followed by procurement of its stromal vascular fraction highly enriched for adipose stem cells, and subsequent combination with synthetic bone substitutes to generate bioactive material for sinus floor elevation
- Primary outcomeSafety: assessment of any AE or SAE related to the product and/or procedure, using patient questionnaires, physical examination, and laboratory measurements
- Secondary outcomeEfficacy: Radiological/clinical assessment of bone height, bone density, and/or bone loss; dental implant integration and survival (assessment by immobility, ankylotic percussion); and histological/histomorphometrical evaluation of biopsies taken 6 months after sinus lifting
- Timepoints- Open Questionnaire and Physical examination: At screening/Inclusion, Baseline (Day 0), and at 1, 6, 9, and 18 months - Laboratory parameters (Haematology, Serum chemistry): At screening/Inclusion, Baseline (Day 0), and at 1 and 6 months - Overall AE and SAE: all visits
- Trial web site
- statusplanned
- CONTACT for SCIENTIFIC QUERIESProf. dr. J. Klein-Nulend
- Sponsor/Initiator VU University Medical Center
- Funding
(Source(s) of Monetary or Material Support)
ZON-MW, The Netherlands Organization for Health Research and Development
- Publications
- Brief summary- So far, ten patients have been uneventfully treated - The one-step surgical procedure in clinical setting is feasible - Safety: So far, no (serious) adverse effects have been observed during follow-up - Efficacy of bone formation: currently being evaluated
- Main changes (audit trail)
- RECORD7-feb-2014 - 11-apr-2014

  • Indien u gegevens wilt toevoegen of veranderen, kunt u een mail sturen naar