Gingival Recession Clinical Trial
Official title:
Mechanisms of LPRF Action in the Promotion of Wound Healing and Tissue Regeneration: A Randomised Controlled Trial
Verified date | February 2023 |
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 intraoral wound healing.
Status | Completed |
Enrollment | 12 |
Est. completion date | December 31, 2022 |
Est. primary completion date | December 30, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Age 18-70 - Non-smokers or former smokers - Participants must agree to read the "Patient information leaflet and provide a signed a copy of the "Informed Consent", after the study design has been completely explained. - Presence of bilateral isolated Miller Class I and II gingival recessions in anterior and premolar regions. - Presence of minimum 2 mm of keratinized gingiva apical to the gingival margin at the selected sites. Exclusion Criteria: - The patient is medically compromised with history of diabetes mellitus or hepatic or renal disease, or other serious medical conditions or transmittable diseases e.g. Hepatitis B or C or AIDS. - History of rheumatic fever, heart murmur, mitral valve prolapse, artificial heart valve or conditions which would require antibiotic prophylaxis invasive dental procedures. - Patients undergoing therapies involving the use of antibiotic, anti-inflammatory or anticoagulant drugs during the month prior to the baseline exam. - History of alcohol use or drug abuse. - Self-reported pregnancy or lactation. - Subjects would be considered inappropriate for the trial if they have a history of pre-existing acute or chronic medical or psychiatric illness and laboratory abnormality which may pose to increase the risk of the subjects involved in the trial or administering the investigational product or may interfere with the interpretation of trial results. |
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 33 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of gingival recession depth (GR) from baseline to 6 months | Measured from the CEJ to the apical extension of the gingival margin in mm with the use of Florida probe. | Baseline, 3 months, and 6 months | |
Primary | Change of probing pocket depth (PPD) from baseline to 6 months | Measured from the gingival margin to base of the gingival sulcus in mm with the use of Florida probe. | Baseline, 3 months, and 6 months | |
Primary | Change of clinical attachment level (CAL) from baseline to 6 months | Measured from cementoenamel junction (CEJ) to the base of the gingival sulcus in mm with the use of Florida probe. | Baseline, 3 months, and 6 months | |
Primary | Change of keratinized mucosa width (KMW) from baseline to 6 months | Measured from the gingival margin to the mucogingival line in mm with the use of Florida probe. | Baseline, 3 months, and 6 months | |
Primary | Change of thickness of keratinised gingiva (GT) from baseline to 6 months | Measured 3 mm apical to the gingival margin in mm measured by superimposition of intraoral digital scanning images. | Baseline, 3 months, and 6 months | |
Secondary | Concentration of gingival wound fluid molecules | Concentration changes of the molecules and inflammatory mediators in the wound fluid (WF). | Baseline, 6 hours, 3 days, and 7 days |
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