Status:
COMPLETED
The Impact of Peri-implant Soft Tissue Properties on Patient-reported and Clinically Assessed Outcomes
Lead Sponsor:
Tufts University
Conditions:
Keratinized Mucosa
Eligibility:
All Genders
18+ years
Brief Summary
The objective of this study is to evaluate patient discomfort while performing oral hygiene (OH) around implants with and without keratinized mucosa (KM) and assess peri-implant soft tissue esthetic s...
Detailed Description
In the oral cavity, the soft tissue of the alveolar ridge can be classified as keratinized mucosa (KM) or alveolar mucosa (AM). Typically KM forms a cuff around an implant, while AM is farther away an...
Eligibility Criteria
Inclusion
- Patients 18 years of age or older
- Patients treatment planned for second stage implant surgery (having already had stage one completed
- Partially or fully edentulous patients that have a single implant or have multiple implants that are non-adjacent
- Patients that have implant(s) that will be restored with fixed cement- or screw-retained restoration(s)
Exclusion
- Unwilling to sign informed consent form
- Non-English speaking subjects
- Pregnant women (self-reported)
- Heavy smokers (10 cigarettes/day)
- Known allergy to iodine and/or potassium iodide (ingredients of Lugol's solution)
Key Trial Info
Start Date :
January 15 2014
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 9 2015
Estimated Enrollment :
43 Patients enrolled
Trial Details
Trial ID
NCT03396536
Start Date
January 15 2014
End Date
June 9 2015
Last Update
March 12 2019
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