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

U

Universitaire Ziekenhuizen KU Leuven

Status

Completed

Conditions

Atrophic Maxilla
Ridge Preservation

Treatments

Other: L-PRF
Other: A-PRF

Study type

Interventional

Funder types

Other

Identifiers

NCT03268512
B322201525149

Details and patient eligibility

About

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.

Enrollment

20 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

20 participants in 3 patient groups

L-PRF
Experimental group
Description:
One socket will be filled with L-PRF membranes and covered with at least 2 L-PRF membranes. A modified horizontal mattress will be place as suture to keep the L-PRF in place.
Treatment:
Other: L-PRF
A-PRF
Experimental group
Description:
One socket will be filled with A-PRF membranes and covered with at least 2 A-PRF membranes. A modified horizontal mattress will be place as suture to keep the A-PRF in place.
Treatment:
Other: A-PRF
Control
No Intervention group
Description:
The socket will be filled with a natural blood clot. A modified horizontal mattress will be place as suture.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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