First experiences with the effectiveness of Geistlich Bio-Oss® Flow (fDBBM-C) in cases of bone defects in the jaw area due to inflammation of the gums in the area of the periodontal apparatus
Summary description of the study
In this study, we investigate the effectiveness of the medical device Geistlich Bio-Oss® Flow in patients with jaw bone defects due to periodontitis. The study takes place at a single center in Switzerland. All patients are treated with Geistlich Bio-Oss® Flow. The duration of study participation is approximately 6 months.
(BASEC)
Intervention under investigation
surgical intervention for jaw bone reconstruction in patients with periodontitis
(BASEC)
Disease under investigation
chronic inflammatory disease of the periodontal apparatus (periodontitis)
(BASEC)
-Patients with a periodontal jaw bone defect (defect depth greater than 3 mm) -Good oral hygiene -Adults 18 years or older (BASEC)
Exclusion criteria
-Active or chronic infections at the surgical site -Clinical condition/treatment affecting tissue healing -Pregnant or nursing women (BASEC)
Trial sites
Bern
(BASEC)
Sponsor
Geistlich Pharma AG
(BASEC)
Contact
Contact Person Switzerland
Stefanie Wolf-Zbinden
+41 41 492 68 24
Stefanie.wolf@cluttergeistlich.comGeistlich Pharma AG Bahnhofstrasse 40 6110 Wolhusen
(BASEC)
Scientific Information
not available
Name of the authorising ethics committee (for multicentre studies, only the lead committee)
Ethics Committee Bern
(BASEC)
Date of authorisation
22.05.2024
(BASEC)
ICTRP Trial ID
not available
Official title (approved by ethics committee)
First experience with the performance of Geistlich Bio-Oss® Flow (fDBBM-C) in periodontal intrabony defects (BASEC)
Academic title
not available
Public title
not available
Disease under investigation
not available
Intervention under investigation
not available
Type of trial
not available
Trial design
not available
Inclusion/Exclusion criteria
not available
not available
Primary and secondary end points
not available
not available
Registration date
not available
Incorporation of the first participant
not available
Secondary sponsors
not available
Additional contacts
not available
Secondary trial IDs
not available
Results-Individual Participant Data (IPD)
not available
Further information on the trial
not available
Results of the trial
Results summary
not available
Link to the results in the primary register
not available