Platelet-Rich Fibrinogen in Extraction Socket Healing of the Aged

ConditionEdentulism
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age14-80
SponsorUniversity of Nebraska

About this trial

The purpose of this study is to better understand oral wound healing in the aged participant following placement of platelet-rich fibrinogen (PRF). In this study, 12 participants requiring a posterior tooth extraction will be enroll: 6 participants aged 14-18, 6 participants aged 50-80. All will undergo a posterior tooth extraction with a small tissue specimen taken from the extraction site. Half of the participants will also have their blood drawn and platelet-rich fibrinogen placed in the extraction socket. Participants will return in 2 weeks for suture removal and another soft tissue sample. Participants will return at 3 months for a final post-operative radiograph. All soft tissue samples will undergo immunofluorescence.

Eligibility criteria

Qualifiers

Patient at University of Nebraska Medical Center (UNMC) College of Dentistry

Requires extraction of posterior tooth

Able and willing to provide consent/assent

Disqualifiers

Systemic conditions that delay wound healing

Chronic use of non-steroidal anti-inflammatory drugs (NSAIDs), methotrexate, bisphosphonates or other drugs that inhibit wound healing Smoking and vaping Pregnancy

Trial design

Treatments tested in this trial

  • Platelet-rich fibrin (PRF)

Treatment groups

12 Participants
are divided into 4 treatment groups

Sponsors and collaborators