ISRCTN98697476
Recruiting
Not Applicable
Clinical, esthetic outcomes and efficiency of the one crown one time concept compared to the conventional approach encompassing soft tissue conditioning for the fabrication of single implant crowns: a pilot randomized controlled multicenter clinical trial
Oral Reconstruction Fundation0 sites32 target enrollmentNovember 21, 2017
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Missing single tooth
- Sponsor
- Oral Reconstruction Fundation
- Enrollment
- 32
- Status
- Recruiting
- Last Updated
- 8 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Older 22 years old
- •2\. Patients with Conelog Implants placed in the anterior and premolar region in the maxilla or mandible.
- •3\. These implants should:
- •3\.1\. Allow for a screw retained reconstruction
- •3\.2\. Be submerged (second stage surgery is the 1st study appointment)
- •4\. Two neighboring teeth are present, or one tooth and one implant
- •5\. Capable of providing written informed consent
- •6\. Obtained informed consent from the patient
- •7\. 2mm band of keratinized mucosa at implant site
- •8\. Patients with adequate oral hygiene Plaque Index \< 20% or persistent intraoral infection BoP \< 20%
Exclusion Criteria
- •1\. Medical condition that contraindicates surgery: ASA \-score \= III
- •2\. History of radiotherapy in the head and neck region
- •3\. History of bisphosphonate medication
- •4\. Women of childbearing potential with a positive urine pregnancy test
- •5\. Medium smokers \= 10 cigarettes per day
- •6\. Patients unwilling or incapable of understanding and signing the informed consent
- •7\. Pronounced esthetic expectations
- •8\. Severe bruxism or clenching habits
Outcomes
Primary Outcomes
Not specified
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