Skip to content

Wound Healing Following Extraction and Ridge Preservation in Smokers and Non-smokers

Wound Healing Following Extraction and Ridge Preservation in Smokers and Non-smokers

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07372183
Enrollment
12
Registered
2026-01-28
Start date
2026-01-25
Completion date
2028-10-01
Last updated
2026-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alveolar Bone Grafting, Bone Healing, Smoking, Cigarette, Tooth Extraction Site Healing, Wound Healing

Brief summary

The goal of this study is to evaluate bone wound healing following extraction and alveolar ridge preservation (bone graft and membrane) clinically, histologically and in relation to gene expression in smokers and non-smokers. Data from a small group of participants will be analyzed after age-matched subjects undergo extraction and alveolar ridge preservation prior to implant placement. The data obtained in this pilot study will be used to plan a full-fledged study involving a larger number of smoking and non-smoking participants to compare the two groups.

Detailed description

All research procedures will start after IRB approval. Patients of the Graduate Periodontics Clinic in need of extraction, bone graft and membrane will be recruited. There will be two groups (smokers and non-smokers) and their demographic and social, periodontal, surgery-related, anatomical and healing variables as well as patient-reported outcomes will be recorded at different time points (immediately before, during and immediately after surgery and 1, 2, 6 weeks and 4 months) in order to evaluate wound healing outcomes and differences between the groups. The demographic and social variables evaluated are age, gender, race, medical history, medications, smoking (via interview and breath test-smokerlyzer) and alcohol consumption (via interview). The periodontal variables are tooth mobility, probing depth, attachment level, gingival and plaque index. The surgery-related variables include intraoperative complications, duration of procedure, anesthetic amount, type and approach and operator experience. The anatomical variables are bone height and width (buccolingual and buccal dimension), bone density (in Cone Beam Computed Tomographies - CBCTs) and gingival width and thickness. The healing variables include wound opening (tested clinically and in photos), bleeding, grafting material discharge, flap necrosis, loose sutures, and temporary restoration adjustment. The patient-reported outcomes are Oral Health Impact Questionnaire-14 (OHIP-14), Visual Analogue Scale (VAS) for pain, swelling and difficulty of mouth opening. At 4 months during the implant placement appointment, a bone core will be harvested via a 3D printed surgical guide based on virtual CBCT planning. The core willl be used of microCT and histological analysis as well as total RNA extraction and RNA sequencing.

Interventions

OTHERobservational study

Observational study; alveolar ridge preservation

Sponsors

Marquette University
Lead SponsorOTHER
LifeNet Health
CollaboratorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Adult patients (18-75 years) * Good general health (controlled conditions) * Smokers (≥10 cigarettes/day for ≥5 years) and never smokers. Confirmation of smoking status will be done via use of a smokerlyzer. The cut-off point for distinguishing smokers from non-smokers is 8 carbon monoxide parts per million (ppm). * Periodontal status: periodontal health, gingivitis on intact or reduced periodontium, treated periodontitis * Intact post-extraction bony walls or less than 50% bone dehiscence * Distance at least 8 mm of vertical bone height between bone crest and anatomical structures (i.e. sinus floor, inferior alveolar nerve (IAN) canal, mental foramen) * Extracted tooth root in the same three-dimensional position as the future implant placement so that the bone core biopsy can be taken from a site totally within the confines of the former tooth socket without inclusion of surrounding native alveolar bone * Scheduled for single tooth extraction with bone graft placement and membrane

Exclusion criteria

* Uncontrolled periodontal disease * Uncontrolled systemic disease * Pregnancy * Use of therapy and/or medication that impairs wound healing (e.g., bisphosphonates, steroids, chemotherapy, radiotherapy etc.)

Design outcomes

Primary

MeasureTime frameDescription
Clinical ParametersMeasured before surgery, during surgery and at 4 monthsbone width

Secondary

MeasureTime frameDescription
Genetic ParametersBone samples harvested at 4 monthsRNA transcriptomic analysis
Histological ParametersSamples harvested at 4 monthsHistological analysis of bone cores: %mineralized bone
Micro-CT ParametersSamples harvested at 4 monthsHistological analysis of bone cores: bone mineral density
Patient-reported ParametersMeasured before surgery, at 1, 2 and 6 weeks, and 4 monthsOral Health Impact Profile -14 (OHIP-14). Range from 0 (no impact) to 56 (most severe impact).

Countries

United States

Contacts

CONTACTVrisiis Kofina, DDS, MS
vrisiis.kofina@marquette.edu516-817-0393
CONTACTMcKenna Schnack, DDS, MS
mckenna.schnack@marquette.edu515-822-3552
PRINCIPAL_INVESTIGATORVrisiis Kofina, DDS, MS

Marquette University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026