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Implant site preparation with conventional rotary drill or piezosurgery: five-year after placement results from a within person randomised controlled trial

Not Applicable
Conditions
Comparison of two different methods of implant site preparation
Registration Number
DRKS00030677
Lead Sponsor
niversitätsmedizin Mainz
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
25
Inclusion Criteria

Non-smokers
-Teeth to be treated: Upper and lower bicuspids and molars
-sufficient bone allowing placement of single implants with a length of at 11 mm and with a diameter of 4.0 mm. Therefore, a crest of at least 12 mm height and 7 mm wide with a healing time after tooth extraction = 6 months
-Full-mouth plaque and bleeding scores =15%, no active periodontal disease and proven ability of the patient for proper oral hygiene
-Signed informed consent form

Exclusion Criteria

general contraindications to implant surgery,
systemic diseases,
immunosuppressed or immunocompromised,
irradiation in the head or neck area,
pregnancy or lactation,
wish for pregnancy,
addiction to alcohol or drugs,
psychiatric disorders,
under treatment or previous treatment with intravenous amino-bisphosphonates,
acute infection in the site intended for implant placement.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Marginal bone loss
Secondary Outcome Measures
NameTimeMethod
Implant stability quotient
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