6 results match your criteria: "University Medical Center of the J.-Gutenberg University[Affiliation]"

Purpose: This non-interventional study investigates variations in the type and frequency of late complications linked to novel zygomatic implant designs, installed adhering to the Zygoma Anatomy-Guided Approach (ZAGA) concept, over an extended follow-up period of at least 3 years.

Methods: Consecutive patients presenting indications for treatment with ZIs were treated according to ZAGA recommendations. Implants were immediately loaded.

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Objectives: The aim of Working Group 3 was to address the influence of both material- and anti-resorptive drug- related factors on clinical and biological outcomes and complications in implant dentistry. Focused questions were addressed on (a) implant materials other than titanium (alloy)s, (b) transmucosal abutment materials and (c) medications affecting bone metabolism were addressed.

Materials And Methods: Three systematic reviews formed the basis for discussion in Group 3.

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Objectives: To systematically assess the literature and report on (1) the frequency of occurrence of buccal soft tissue dehiscence (BSTD) at implants, (2) factors associated with the occurrence of BSTD and (3) treatment outcomes of reconstructive therapy for the coverage of BSTD.

Materials And Methods: Two systematic reviews addressing focused questions related to implant BSTD occurrence, associated factors and the treatment outcomes of BSTD coverage served as the basis for group discussions and the consensus statements. The main findings of the systematic reviews, consensus statements and implications for clinical practice and for future research were formulated within group 3 and were further discussed and reached final approval within the plenary session.

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Introduction: There are few zygomatic implants (ZI) designs available. The objective of this non-interventional study was to report the effectiveness of two new site-specific ZI, selected and placed following the zygoma anatomy-guided approach (ZAGA).

Materials And Methods: Consecutive patients presenting indications for rehabilitation using ZI were treated according to ZAGA Concept recommendations.

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Position-dependent accommodative shift of retropupillary fixated iris-claw lenses.

Graefes Arch Clin Exp Ophthalmol

December 2012

Department of Ophthalmology, University Medical Center of the J.-Gutenberg University, Langenbeckstr. 1, 55131, Mainz, Germany.

Purpose: After implantation of retropupillary fixated iris-claw lenses, changes of the objective refraction can occur depending on the patients' position. The purpose of this study was to evaluate and quantify these changes as well as the influencing factors.

Methods: Within a retrospective study, postoperative refraction visual, acuity and anterior chamber depth after implantation of a retropupillary fixated iris-claw lens (Artisan® / Verisyse®) were measured in 51 eyes (49 patients) depending on their head position.

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Multicenter randomized clinical trial: early loading of implants in maxillary bone.

Clin Implant Dent Relat Res

October 2013

Medical director, Department of Oral and Maxillofacial Surgery, Plastic Operations, University Medical Center of the J. Gutenberg University, Mainz, Germany; head of department, Department of Medical Biometry and Epidemiology, Faculty for Health, Witten/Herdecke University, Witten, Germany; private practice, Münster, Germany; medical director, Department of Cranio-Maxillofacial Surgery, University Hospital Muenster, Muenster, Germany; head of department, Department of Maxillofacial Surgery, University of Erlangen, Erlangen, Germany; private practice, Stuttgart, Germany; medical director, Department of Maxillofacial Surgery, University of Erlangen, Erlangen, Germany; head of department, Department for Oral and Maxillofacial Surgery, Katharinenhospital, Stuttgart, Germany; head of department, Department of Oral and Maxillofacial Surgery, Plastic Operations, University Medical Center of the J. Gutenberg University, Mainz, Germany.

Purpose: The aim of this study was to show prognostic equivalence between implant loading in the maxilla after 12 weeks versus 4 weeks.

Materials And Methods: One hundred four patients, from four centers in this open-labeled randomized multicenter prospective controlled clinical trial, were assigned to either 12 weeks or 4 weeks of unloaded healing. Two hundred sixty-nine implants (sand blasted large-grid, acid etched [SLA] surface, ≥ 4.

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