About this trial
Patients presenting to the University of Nebraska Medical Center College of Dentistry for a posterior extraction will be offered participation in the study. Prior to extraction, subjects will undergo clinical measurements, xray, gingival crevicular fluid (GCF) and saliva sampling and a blood draw. Following atraumatic tooth extraction, the subjects will be reevaluated for healing at 1, 2-weeks and 3 months. At each appointment, GCF, saliva and wound fluid (WF) will be collected and at 3 months a second xray will be taken.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
needs posterior tooth extracted
no systemic conditions or meds affecting wound healing
non-smoker
Disqualifiers
systemic conditions or meds known to affect wound healing
smokers
Trial population
Study population will be made of patients at the UNMC College of Dentistry requiring posterior extraction, aged 65-80.
Trial design
Cohort
Prospective
Treatments tested in this trial
tooth extraction
Procedure/Surgeryposterior tooth extraction
Treatment groups
Trial outcomes
Primary outcomes
Amount of Interleukin-1 beta (IL1-B) in gingival crevicular at baseline
Measurement of IL1B in GCF
Secondary outcomes
Bone Density
Change in bone density post-extraction
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: