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Evaluation of the Effect of Leucocyte Platelet-Rich Fibrin (L-PRF) Technique Applied in Post-extraction Sockets Before Placement of Dental Implants

Evaluation of the Effect of Leucocyte Platelet-Rich Fibrin (L-PRF) Technique Applied in Post-extraction Sockets Before Placement of Dental Implants

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07387913
Enrollment
40
Registered
2026-02-04
Start date
2022-09-05
Completion date
2026-09-15
Last updated
2026-02-04

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

Conditions

L-PRF, Dental Implants, Osseointegration, Alveolar Bone Grafting

Keywords

Dental implant, Platelet-rich fibrin, Alveolar ridge preservation, Dental implant stability, Tooth-socket preservation

Brief summary

Aim of study: The application of L-PRF membrane in post-extraction sockets outmatches the use of a) allograft covered with a collagen fleece b) allograft combined with L-PRF membrane c) natural healing, with reference to bone remodeling and regeneration of post-extraction sockets. Moreover, it will be examined whether the application of L-PRF membrane leads to faster bone maturation and creation of a favorable biological environment for earlier implant placement. Materials and methods: This study is taking place in Athens University Dental School, in Oral and Maxillofacial Surgery Clinic. All patients participating in the present study received thorough informed consent. All forty patients participating in this study, were subjected in at least one atraumatic and flapless extraction of a single rooted tooth in the maxilla or mandible. Then, the patients were randomly divided in four categories with regards to management of the socket: a) no intervention i.e. Natural healing b) application of L-PRF membrane in the socket c) application of allograft (Phoenix) covered with a collagen fleece d) application of allograft (Phoenix) covered with a L-PRF membrane. Interrupted sutures will be performed for the four extraction socket groups. Radiographic examination (localized CBCT) was obtained immediately before the extraction, as well as three months post-operatively (localized CBCT) in order to assess the changes in the alveolar ridge dimensions. The next stage of the study refers to the rehabilitation of the edentulous region. Before each patient was subjected to dental implant placement, a bone biopsy was obtained. Therefore, all the biopsy specimens obtained went through histological evaluation in order to assess qualitative and quantitative features.

Interventions

PROCEDUREAllograft and collagen membrane

The post-extraction sockets will be filled with allograft particles and collagen membrane.

PROCEDUREAllograft and L-PRF membrane

The post-extraction sockets will be filled with allograft particles and L-PRF membrane.

PROCEDUREL-PRF

The post-extraction sockets will be filled with L-PRF membrane.

Sponsors

National and Kapodistrian University of Athens
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

1. Single-rooted teeth needed to be extracted in the maxilla or mandible 2. Patient in good general health as documented by self-assessment 3. Patients must be committed to the study and sign the informed consent 4. Adults only as participants

Exclusion criteria

1. No systemic medical condition that could interfere with the surgical procedure or planned treatment. 2. Smokers \>20 cig/day 3. Current pregnancy or breast feeding 4. Radiotherapy or chemotherapy in head and neck area intravenous and oral bisphosphonates or anti-angiogenic drugs

Design outcomes

Primary

MeasureTime frameDescription
Radiographic assessment of the bone specimens3 monthsComparison of quantitative clinical alveolar ridge dimensions (in mm) between the four groups will be performed, 3 months after alveolar ridge preservation. Radiographic evaluation will take place and changes in horizontal dimension will be measured. The horizontal bone width of the ridge at the time of the extraction and after 3 months during the implant placement procedure will be measured in mm.

Secondary

MeasureTime frameDescription
Radiographic assessment of the bone specimens3 monthsComparison of quantitative clinical alveolar ridge dimensions (in mm) between the four groups will be performed, 3 months after alveolar ridge preservation. Radiographic evaluation will take place and changes in vertical dimension will be measured. The vertical bone height of the ridge at the time of the extraction and after 3 months during the implant placement procedure will be measured in mm.
Histological assessment of the bone harvested from the post-extraction sockets3 monthsMeasure quantitative histologic characteristics of new bone formation between the four groups after 3 months of alveolar ridge preservation by quantifying the distribution in (%) of new vital bone formed at the healed socket site.

Countries

Greece

Contacts

STUDY_CHAIRNadia Lygidakis, Associate Professor

National and Kapodistrian University of Athens

Outcome results

None listed

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