Evidence map›Paper›PMID 36826514›Full record

Trial reportClinical oral investigations2023

A novel porcine dentin-derived bone graft material provides effective site stability for implant placement after tooth extraction: a randomized controlled clinical trial.

Lari Sapoznikov, Doron Haim, Barbara Zavan, Gérard Scortecci, Martin F Humphrey

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical oral investigations, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03150472 (Safety and Efficacy Evaluation of the Ivory Dentin Graft Device), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03150472 nacompletednot on this map

Safety and Efficacy Evaluation of the Ivory Dentin Graft Device

TypeinterventionalSponsorIvory Graft Ltd.Ran2017 to 2020Enrolled43ConditionsDeficiency of Alveolar Ridge (Disorder), Alveolar Bone Grafting, Mandibular Prosthesis UserArmsGraft Matrix
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 3 countries.

Lari SapoznikovPrivate Practice, Tel Aviv, Israel.
Doron HaimShamir Medical Center, 70300, Zerifin, Israel.
Barbara ZavanDepartment of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Gérard ScortecciBasal Implantology Program, Department of Maxillo-Facial Surgery, School of Medicine, University Côte d'Azur, 06000, Nice, France.
Martin F HumphreyPrivate Consultant, Keferstrasse 33, 80802, Munich, Germany. consulting@mhumphrey.de.
Assaf Harofeh Medical Center · ILCognition Behaviour Technology · FRUniversity of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAssessment of the clinical performance of a porcine dentin-derived particulate bone graft material for bone regeneration after tooth extraction with implant placement at 4 months, in comparison to a commercially available porcine bone-derived graft. MATERIAL AND

methodsThis study was a randomized, parallel-group, semi-double-blinded clinical trial evaluating the clinical safety, tolerability, and performance of Ivory Dentin Graft™ in comparison with a commercial bone-derived material in alveolar ridge preservation following tooth extraction (registered at ClinicalTrials.gov, May 12th, 2017, Identifier NCT03150472). Extraction sites were grafted with test or comparator material and a titanium implant placed at 4 months after taking a graft site biopsy. Primary endpoints were the extent of new bone growth and bone-graft integration at 4 months.

resultsThe dentin graft material had statistically significantly more new bone formation (60.75% vs 42.81%, p = 0.0084, N = 20 vs 16), better bone-graft integration scores (good integration in 85% vs 40%, p = 0.0066), and higher mean radiodensity of the bone (981.5HU vs 727.7HU, p = 0.0011) at the graft site compared to the bone-derived material. The mean implant insertion torque force was similar for the dentin and bone materials (34.75 Ncm vs 34.06 Ncm). Titanium implant placement was successful in 95% of patients with the dentin graft material compared to 81.25% for the bone graft. Both materials had similar clinical safety and tolerability as determined by adverse events and local site reactions. Physician-assessed ease of grafting and ease of implant placement on a 10-point scale showed no statistical differences (8.78 vs 8.27, p = 0.2355; 8.05 vs 8.75, p = 0.1118, respectively).

conclusionsA porcine dentin-derived bone graft material has clinical safety, tolerability, and performance for implant placement at 4 months after tooth extraction at least as good as a commercial bone-derived material. CLINICAL RELEVANCE: The availability of porcine dentin-derived bone graft material allows wider use of dentin-derived material which has so far only been available in the form of autologous dentin from the patient's own teeth.

Indexed as

Alveolar Ridge AugmentationBone SubstitutesDental ImplantsAnimalsBone TransplantationDental Implantation, EndosseousDentinHumansSwineTitaniumTooth ExtractionTooth SocketTreatment OutcomeBone SubstitutesDental ImplantsTitaniumAlveolar bone lossBone substitutesClinical trialDental implantsDentin

Identifiers

PMID36826514
PMCPMC10264522
OpenAlexW4321748319

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.