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A phase IIa randomized controlled pilot study evaluating the safety and clinical outcomes following the use of rhGDF-5/β-TCP in regenerative periodontal therapy

cris.virtualsource.author-orcidddeb752c-6f59-466e-a26d-7e9b0a6d84d4
datacite.rightsopen.access
dc.contributor.authorWindisch, Péter
dc.contributor.authorStavropoulos, Andreas
dc.contributor.authorMolnár, Bálint
dc.contributor.authorSzendröi-Kiss, Dóra
dc.contributor.authorSzilágyi, Emese
dc.contributor.authorRosta, Péter
dc.contributor.authorHorváth, Attila
dc.contributor.authorCapsius, Björn
dc.contributor.authorWikesjö, Ulf M E
dc.contributor.authorSculean, Anton
dc.date.accessioned2024-10-11T13:03:41Z
dc.date.available2024-10-11T13:03:41Z
dc.date.issued2012
dc.description.abstractTo present the safety profile, the early healing phase and the clinical outcomes at 24 weeks following treatment of human intrabony defects with open flap debridement (OFD) alone or with OFD and rhGDF-5 adsorbed onto a particulate β-tricalcium phosphate (β-TCP) carrier. Twenty chronic periodontitis patients, each with at least one tooth exhibiting a probing depth ≥6 mm and an associated intrabony defect ≥4 mm entered the study. Ten subjects (one defect/patient) were randomized to receive OFD alone (control) and ten subjects OFD combined with rhGDF-5/β-TCP. Blood samples were collected at screening, and at weeks 2 and 24 to evaluate routine hematology and clinical chemistry, rhGDF-5 plasma levels, and antirhGDF-5 antibody formation. Plaque and gingival indices, bleeding on probing, probing depth, clinical attachment level, and radiographs were recorded pre- and 24 weeks postsurgery. Comparable safety profiles were found in the two treatment groups. Neither antirhGDF-5 antibody formation nor relevant rhGDF-5 plasma levels were detected in any patient. At 6 months, treatment with OFD + rhGDF-5/β-TCP resulted in higher but statistically not significant PD reduction (3.7 ± 1.2 vs. 3.1 ± 1.8 mm; p = 0.26) and CAL gain (3.2 ± 1.7 vs. 1.7 ± 2.2 mm; p = 0.14) compared to OFD alone. In the tested concentration, the use of rhGDF-5/β-TCP appeared to be safe and the material possesses a sound biological rationale. Thus, further adequately powered, randomized controlled clinical trials are warranted to confirm the clinical relevance of this new approach in regenerative periodontal therapy. rhGDF-5/β-TCP may represent a promising new techology in regenerative periodontal therapy.
dc.description.numberOfPages9
dc.description.sponsorshipZahnmedizinische Kliniken, Klinik für Parodontologie
dc.identifier.doi10.7892/boris.11264
dc.identifier.isi000306590000021
dc.identifier.pmid21887500
dc.identifier.publisherDOI10.1007/s00784-011-0610-3
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/81443
dc.language.isoen
dc.publisherSpringer-Verlag
dc.publisher.placeBerlin
dc.relation.ispartofClinical oral investigations
dc.relation.issn1432-6981
dc.relation.organizationDCD5A442B9BDE17DE0405C82790C4DE2
dc.titleA phase IIa randomized controlled pilot study evaluating the safety and clinical outcomes following the use of rhGDF-5/β-TCP in regenerative periodontal therapy
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage9
oaire.citation.issue4
oaire.citation.startPage1181
oaire.citation.volume16
oairecerif.author.affiliationZahnmedizinische Kliniken, Klinik für Parodontologie
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unibe.date.licenseChanged2019-10-22 17:39:03
unibe.description.ispublishedpub
unibe.eprints.legacyId11264
unibe.journal.abbrevTitleCLIN ORAL INVEST
unibe.refereedtrue
unibe.subtype.articlejournal

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