Actively Recruiting

Age: 21Years - 70Years
All Genders
Healthy Volunteers
ID04805320

Association of Periodontal Inflammation on Immune Response in Wound Healing after Posterior Tooth Extraction

Led by University of Nebraska · Updated on 2025-12-10

25

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand how inflammation in the mouth affects the immune response during wound healing after tooth extraction. The study involves healthy adults aged 21 to 70 who need a posterior tooth extracted. Researchers will measure periodontal inflammation and take dental X-rays before the extraction to gather baseline information. Participants will undergo an atraumatic extraction of the affected tooth using local anesthesia. Small soft tissue biopsies from the extraction site will be collected immediately after extraction and again two weeks later when sutures are removed. A final visit at three months post-extraction will include clinical assessments and dental X-rays to evaluate healing. Throughout the study, researchers will collect data such as probing depths, gum recession, bleeding, and fluid samples from adjacent teeth. The soft tissue samples will be analyzed to count inflammatory cells and study immune activity during healing. Participants will be involved in three main visits over about three months, with careful monitoring of healing and inflammation.

CONDITIONS

Brief Title

Association of Periodontal Inflammation on Immune Response in Wound Healing

Who Can Participate

Age: 21Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult aged 21 to 70 years
  • Have a non-restorable posterior tooth (molar or premolar) needing extraction
Not Eligible

You will not qualify if you...

  • Presence of systemic disease that affects inflammation and wound healing processes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Dental Extraction and Immediate Post-operative Care

Duration - 1 day

Participants undergo extraction of a posterior tooth with local anesthesia, followed by a soft tissue biopsy and suturing of the extraction site.

1 visit (in-person)

Post-operative Follow-up

Duration - 2 weeks

Participants return at two weeks for suture removal and a second soft tissue biopsy, along with clinical assessments of the healing site and adjacent teeth.

1 visit (in-person)

Long-term Monitoring

Duration - 3 months

At three months post-extraction, participants have clinical evaluations of wound healing, including inflammatory measures and radiographic imaging of the adjacent teeth and extraction site.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

University of Nebraska, College of Dentistry

Lincoln, Nebraska, United States, 68583

Actively Recruiting

Loading map...

Research Team

A

Amy C Killeen, DDS

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here