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Clinical Trials/NL-OMON50613
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

Vrije Universiteit0 sites43 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

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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