At a glance
ClinicalIndex Comparison RecordN/ACompleted· 14 enrolled
Drug / intervention
Straumann BoneCeramic +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Randomised Controlled Spilt-mouth Clinical Study Comparing a Synthetic Bone Substitute and a Bovine-derived Xenograft in Primarily Horizontal Bone Augmentation Procedure During Placement of Straumann Oral Implants
In Brief
A clinical study evaluating Straumann BoneCeramic and Bio-Oss for Jaw, Edentulous and Jaw, Edentulous, Partially. Completed, enrolled 14 participants across 1 site.
Detailed Summary
The objective of the study is to test the efficacy on bone formation of Straumann Bone Ceramic as a grafting material applied in buccal bone dehiscences on simultaneously placed oral implants.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsJaw, Edentulous, Jaw, Edentulous, Partially
CountriesBelgium
Collaborators--
Timeline
N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartMar 2006
Primary CompletionFeb 2008
Study CompletionAug 2008
First PostedMay 2009
TodayJul 2026
First PostedMay 13, 2009
Enrollment StartMar 1, 2006
Primary CompletionFeb 1, 2008
Study CompletionAug 1, 2008
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 17.1 years ago
Interventions
Straumann BoneCeramicdevice
Bone augmentation procedure performed with Bone Ceramic
Bio-Ossdevice
Bone Augmentation procedure performed with Bio Oss