NL-OMON50613
Recruiting
Not Applicable
Comparison of clinical and radiographical outcomes following placement of hybrid and moderate rough implants in the posterior mandible of periodontally compromised patients: a 3-year randomized clinical trial - Comparison of hybrid and rough implants in perio patients
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Vrije Universiteit
- Enrollment
- 43
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Periodontally compromised patients having a history of proximal attachment
- •loss of \> 5mm in \> 30% of teeth present
- •\- Enrolled in a supportive periodontal therapy (SPT) program after active
- •periodontal treatment
- •\- Requirement of two single\-unit FPDs supported by two implants in mandibular
- •premolar/molar area
- •\- Adjacent tooth/teeth must have natural root(s)
- •\- In antagonist jaw natural teeth, partial prosthesis, or implants supported
- •(partial) prosthesis in contact with planned FPD
- •\- History of edentulism in planned implant areas \> 4 months
Exclusion Criteria
- •\- History of local radiotherapy to the head and neck region
- •\- History of chemotherapy \< 5 years prior to surgery
- •\- Smoking \> 10 cigarettes a day
- •\- Uncontrolled diabetes mellitus
- •\- Known or suspected current malignancy
- •\- Pregnancy at time of inclusion
- •\- Alcohol or drug abuse
- •\- Any systemic or local disease that would compromise postoperative healing
- •and/or osseointegration
- •\- Need for systemic bisphosphonates, corticosteroids or any other medication
Outcomes
Primary Outcomes
Not specified
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