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Effect of L-PRF and A-PRF in Ridge Preservation

The Use of L-PRF and A-PRF in Ridge Preservation: a Randomized Controlled Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03268512
Enrollment
20
Registered
2017-08-31
Start date
2015-08-22
Completion date
2018-10-10
Last updated
2018-10-11

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

Conditions

Atrophic Maxilla, Ridge Preservation

Keywords

leucocyte- and platelet rich fibrin, ridge preservation, growth factors, platelet concentrates

Brief summary

A split-mouth design study will be performed regarding the use of platelet concentrates on ridge preservation: L-PRF vs A-PRF vs control. Patient needing multiple teeth extractions in the upper jaw (single-rooted teeth) will be recruited. The use of each platelet concentrate or control will be randomized by means of a computer program. The results will be analysed clinical and radiographically (CBCT). When the subject will choose for implant rehabilitation, a biopsy will be taken in the site of the preserved sockets. The region will be localized with a customized stent, fabricated with the position of the extracted teeth. VAS scales will be provided to evaluate the post-operative discomfort.

Interventions

OTHERL-PRF

Platelet concentrates are produced from a small peripheral blood sample, which is immediately centrifuged without any anticoagulant. Coagulation starts during the centrifugation, and three layers are obtained: red blood corpuscles (RBCs) at the bottom of the tube, platelet-poor plasma (PPP) on the top and an intermediate layer called buffy coat where most platelets and leucocytes are concentrated. L-PRF has potential advantages, namely: it creates a bioactive construct that stimulates the local environment for differentiation and proliferation of stem and progenitor cells and it acts as an immune regulation node with inflammation control abilities, such as slow continuous release of growth factors over a period of 7-14 days.

OTHERA-PRF

Platelet concentrates are produced from a small peripheral blood sample, which is immediately centrifuged without any anticoagulant. Coagulation starts during the centrifugation, and three layers are obtained: red blood corpuscles (RBCs) at the bottom of the tube, platelet-poor plasma (PPP) on the top and an intermediate layer called buffy coat where most platelets and leucocytes are concentrated. L-PRF has potential advantages, namely: it creates a bioactive construct that stimulates the local environment for differentiation and proliferation of stem and progenitor cells and it acts as an immune regulation node with inflammation control abilities, such as slow continuous release of growth factors over a period of 7-14 days.

Sponsors

Universitaire Ziekenhuizen KU Leuven
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 80 Years
Healthy volunteers
Yes

Inclusion criteria

* 3 single-rooted teeth needed to be extracted in the upper jaw * patient in good general health as documented by self-assessment * patients must be committed to the study and must be willing to sing the informed consent.

Exclusion criteria

* any systemic medical condition that could interfere with the surgical procedure or planned treatment. * current pregnancy or breast feeding * radiotherapy or chemotherapy in head and neck area * intravenous and oral bisphosphonate * patients smoking \>20 cig/day * unwillingness to return for the follow-up examination

Design outcomes

Primary

MeasureTime frameDescription
Changes horizontal width at crest -1mm3 monthsPrimary outcome variables were defined as the changes in horizontal width at crest-1 mm levels.

Secondary

MeasureTime frameDescription
Changes horizontal width at crest -3 mm and 5 mm; vertical resorption; socket fill3 monthsChanges in horizontal width at crest -3 mm and 5 mm; vertical resorption at the lingual and buccal side; socket fill.

Other

MeasureTime frameDescription
Post-operative scores1 weekPost-operative discomfort measured with VAS

Countries

Belgium

Outcome results

None listed

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