Nova Southeastern University
Fort Lauderdale, Florida, 33328, United States
Location status: Recruiting
NCT Number: NCT06275789
The purpose of the study is to compare a new grafting material for alveolar ridge preservation to a commonly used and well studied material. Alveolar ridge dimensions as well as histology will be compared.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Fort Lauderdale, Florida, 33328, United States
Location status: Recruiting
Brief Background and Goal: Dimensional changes following extractions are inevitable. Many techniques and combinations of materials have been studied and shown to be effective at minimizing these changes. Although no material has been able to fully preserve the ridge, xenografts have been shown to be the most effective at maintaining the volume, however, the use of demineralized freeze-dried bone allograft (DFDBA) results in the most vital bone when evaluated histologically. These factors are important when planning for a successful future implant supported prosthesis. A new material that combines xenograft (deproteinized bovine bone mineral - DBBM) with DFDBA has recently been introduced to the market. The aim of the study is to compare the dimensional and histological changes following flapless alveolar ridge preservation (ARP) in the premolar and molar region with a new material that combines DFDBA and DBBM to a commonly used mineralized allograft.
Research Question: In patients who require an extraction for future implant placement, during alveolar ridge preservation, will combining demineralized freeze-dried bone allograft (DFDBA) and deproteinized bovine bone mineral (DBBM) compared to Tutoplast® processed mineralized particulate allograft result in less dimensional changes at the time of implant placement 4 months later.
Specific Aims: The primary goal of the study is to compare the dimensional changes following alveolar ridge preservation with a new material that combines DFDBA and DBBM to a commonly used mineralized allograft material. The secondary goal is to assess the histological composition of the bone after 4 months of healing. The additional goals are to measure possible confounding factors on the dimensional changes of the alveolar ridge.
Significance: The goal behind the combination of DBBM and DFDBA is to evaluate whether there could potentially be a synergistic effect between the two materials that would make it a more desirable material to use for ARP procedures.
Innovation: There is currently no published research that compares the combination of DFDBA and DBBM to a conventional method inside the extraction site during an alveolar ridge preservation procedure. This grafting material is new on the market and the first of its kind.
Research Plan: The randomized clinical trial will be performed at the Nova Southeastern College of Dental Medicine in the Post-graduate Periodontology Clinic. 30 patients requiring premolar or molar extraction with future implant placement will be randomly divided into 2 groups, one test and one control. Following extraction, the patients will receive either allograft or graft combination of DFDBA and DBBM. The changes in horizontal and vertical dimensions of the alveolar ridge as well as the histology will be assessed and compared at 4 months.
Expected Results: When compared to allograft, the graft mixture containing the DFDBA and DBBM will maintain greater dimensional volume due to the dimensionally stable properties of DBBM and will contain more vital bone due to the osteoinductive properties of DFDBA.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Premolar tooth will be extracted flapless and ridge preservation procedure with bone grafting material will be done.
Time frame: 4 months
Soft and hard tissue horizontal dimensions of the alveolar ridge will be measured after extraction and 4 months later.
Time frame: 4 months
Soft and hard tissue vertical dimensions of the alveolar ridge will be measured after extraction and 4 months later.
Time frame: 4 months
vital bone percentage will evaluated histologically following biopsy at time of implant placement.
Time frame: 4 months
the thickness of the buccal plate will be measured digitally to assess if it may be a confounding factor
Time frame: 4 months
the thickness of the lingual plate will be measured digitally to assess if it may be a confounding factor
Time frame: 4 months, 1 year
the thickness of the overlying soft tissue will be measured digitally to assess if it may be a confounding factor
Time frame: 4 months, 1 year
the position of the tooth in the arch will be analyzed to assess if it may be a confounding factor
Time frame: 4 months
the quantity of cigarettes will be analyzed to assess if it may be a confounding factor
Time frame: 4 months, 1 year
the effectiveness of oral hygiene will be analyzed to assess if it may be a confounding factor
Contact information is provided by the study sponsor or research team.
Andee Goldstein, DMD
CONTACT
Fatemeh Samavatijame, DMD
CONTACT
(734) 546-9018
Nova Southeastern University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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