MedPath

Horizontal ridge augmentation using porcine grafting material and shell technique - a prospective volumetric and histological study

Not Applicable
Conditions
K08.2
Atrophy of edentulous alveolar ridge
Registration Number
DRKS00027922
Lead Sponsor
niversitätsklinik für Zahn, Mund- und Kieferheilkunde Klinik für Mund-, Kiefer- und Gesichtschirurgie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
20
Inclusion Criteria

Patients who receive augmentation and implant treatment due to medical indication.
- People over the age of 20 in the sense of the age of majority, as well as full legal capacity (§§ 2 BGB).
- Patients who have received and signed the form of consent befor the beginning of the treatment.
- Patients who have been told, that the augmentation material has a porcine source and have given consent to be treated with MinerOss.
- Non-smokers or moderate smokers (= 20 cigarettes a day)
- Good oral hygiene and plaque control of the patient (FMPS = 25%)

Exclusion Criteria

- General diseases that can affect healing after implantation or augmentation.
- Diseases of mucous membrane (e.g. erosive lichen planus)
- Patients after radiotherapy
- untreated gingivitis or periodontitis
- untreated endodontic lesions
- probing of the PD = 4mm directly adjacent to the planned implant position
- heavy smokers (> 20 cigarettes a day) or consumers of chewing tabacco
- Pregnant or breastfeeding women
- Patients who out of religious reasons don´t want to be treated with a use of animal/porcine products

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Histological and volumetric evaluation of bone augmentation rate using MinerOss XP and SonicWeld shell 4 months after augmentation.
Secondary Outcome Measures
NameTimeMethod
Wound dehiscence rate after augmentation with MinerOss XP and SonicWeld Rx shell.
© Copyright 2025. All Rights Reserved by MedPath