Tooth Extraction Clinical Trial
Official title:
The Clinical and Biological Effects of Leucocyte and Platelet-rich Fibrin (L-PRF) on Post-extraction Sockets Healing: a Randomized Controlled Trial
Verified date | January 2022 |
Source | The European Research Group on Periodontology (ERGOPerio) |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study evaluates the clinical and biological effects of leucocyte and platelet-rich fibrin (L-PRF) on post-extraction sockets healing.
Status | Completed |
Enrollment | 18 |
Est. completion date | December 31, 2021 |
Est. primary completion date | December 31, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Participant is willing and able to give informed consent for participation in the study - Healthy males and females of age 18-70 - Need for two or more extractions of single rooted teeth in the presence of adjacent teeth or implants due to unrestorable caries, residual roots, root fractures or orthodontic treatment - Able (in the investigators opinion) and willing to comply with all study requirements - Interested in tooth replacement with dental implants Exclusion Criteria: - Endodontic periapical lesions with a diameter of more than 5 mm (radiographically determined) - Sites with buccal and lingual bone plate loss more than 5 mm - Frank purulence or acute abscess at the time of extraction - Pregnancy or lactation - Smokers or alcoholics - Platelet dysfunction syndrome or thrombocytopenia - Uncontrolled diabetes - Medical contraindications to elective oral surgery procedures |
Country | Name | City | State |
---|---|---|---|
Hong Kong | Faculty of Dentistry, The University of Hong Kong | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
The European Research Group on Periodontology (ERGOPerio) | The University of Hong Kong |
Hong Kong,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Concentrations changes of the molecules and inflammatory mediators | Concentrations changes of the molecules and inflammatory mediators in the gingival crevicular fluid (GCF) or wound fluid (WF) from the extraction sockets in L-PRF group and control group at baseline (from GCF), 6 hours, 24 hours, 3 days, 7 days. | Baseline, 6 hours, 24 hours, 3 days and 7 days | |
Secondary | Genes expression profiles | Genes expression profiles of the growth and differentiation factors and inflammatory mediators from the tissue specimen taken from the post-extraction sockets at 3 days. | Baseline and 3 days | |
Secondary | Laser Doppler Flowmetry (LDF) measurement | A commercially available Laser Doppler Blood FlowMeter equipped with a standard fiber optic probe will be used for LDF measurements before tooth extraction, immediately postoperatively, 6 hours, 24 hours, 3 days and 7 days. | Before and immediately after the tooth extraction, 6 hours, 24 hours, 3 days and 7 days | |
Secondary | Radiographic bone changes (Cone-beam computed tomography) | Cone-beam computed tomography (CBCT) images will be obtained before extraction as the baseline and at the 4 months. | Baseline and 4 months | |
Secondary | Wound Healing Index (HI) | Soft tissue healing will be assessed by Wound Healing Index (1 = very poor, 2 = poor, 3 = good, 4 = very good, 5 = excellent). | 6 hours, 24 hours, 3 days and 7 days | |
Secondary | Visual analog scale (VAS) | A 10-point VAS with a score of 0 that equals "no pain" and a score of 10 that equals "worst pain imaginable" will be used to evaluate the postoperative pain at 6 hours, 24 hours, 3 days and 7 days. The patients will be asked to fill the pain they feel at the time of questioning. Questionnaires will be collected at the one-week follow-up visit. | 6 hours, 24 hours, 3 days and 7 days |
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