Advanced PRF vs PRF for Gap Filling in Immediate Implants

NCT07319494 — Not applicable, Active not recruiting, 16 participants, Beni-Suef University

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Comparison of Advanced Platelet Rich Fibrin Versus Platelet Rich Fibrin as a Gap Filling Material in Immediate Implant Placement

RegistryNCT07319494, acronym A-PRF vs PRF
StatusActive not recruiting
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: none, treatment
Enrollment16 (Actual)
SponsorBeni-Suef University (Other)
ConditionsComparison of Advanced Platelet-Rich Fibrin Versus Platelet-Rich Fibrin as a Gap-filling Material
InterventionsImmediate Dental Implant and A-PRF, Immediate dental implant and PRF (Procedure)
Datesstart 2025-06-25, primary completion 2025-11-26, completion 2026-02-15 (estimated), first posted 2026-01-06, last updated 2026-01-06
Locations1 site in Egypt

Related Papers Related Patents Related Grants Related Experts
All trials for Comparison of Advanced Platelet-Rich Fibrin Versus Platelet-Rich Fibrin as a Gap-filling Material All trials of Immediate Dental Implant and A-PRF All trials of Immediate dental implant and PRF

-Summary

Study type: Clinical Trial

Goal:

The goal of this clinical trial is to learn if Advanced Platelet-Rich Fibrin (A-PRF) versus traditional Platelet-Rich Fibrin (PRF) can improve bone healing and soft tissue outcomes in patients undergoing immediate dental implant placement.

Main questions it aims to answer:

Does A-PRF provide greater buccal bone preservation compared to PRF after immediate implant placement?

Does A-PRF improve soft tissue healing and reduce postoperative complications compared to PRF?

Comparison group:

Researchers will compare A-PRF to PRF as a gap-filling material in immediate implants to see if A-PRF results in better bone and soft tissue outcomes.

Participants will:

Undergo tooth extraction followed by immediate implant placement

Receive either A-PRF or PRF as the gap-filling material in the implant site

Have CBCT scans at baseline and 6 months to measure bone thickness

Have clinical assessments of soft tissue healing and implant stability

Attend follow-up visits at 1 week, 1 month, 3 months, and 6 months post-surgery

Expand all sections  ·  Collapse all

+Arms and interventions

ArmTypeInterventionsDescription
PRF GroupExperimentalProcedure: Immediate dental implant and PRFParticipants in this arm will undergo tooth extraction followed by immediate implant placement. The extraction socket will be filled with traditional Platelet-Rich Fibrin (PRF) as the gap-filling material.
A-PRF GroupExperimentalProcedure: Immediate Dental Implant and A-PRFParticipants in this arm will undergo tooth extraction followed by immediate implant placement. The extraction socket will be filled with Advanced Platelet-Rich Fibrin (A-PRF) as the gap-filling material.
  • Immediate Dental Implant and A-PRF (Procedure): Arm 1: Advanced Platelet-Rich Fibrin (A-PRF) Participants will have a tooth extracted, the socket cleaned, and A-PRF prepared from their blood placed in the socket as a gap-filling material before immediate implant placement. Follow-up visits will assess bone and soft tissue healing and implant stability.
  • Immediate dental implant and PRF (Procedure): Arm 2: Platelet-Rich Fibrin (PRF) Participants will have a tooth extracted, the socket cleaned, and traditional PRF prepared from their blood placed in the socket as a gap-filling material before immediate implant placement. Follow-up visits will assess bone and soft tissue healing and implant stability.

+Outcome measures

Primary outcomes

  • Clinical evaluation [6 month]: Implant stability will be measured by resonance frequency analysis (RFA) values expressed as implant stability quotient (ISQ) unit at 6 months post-operative

+Eligibility

Sex: All, ages: 20 Years to any

Inclusion Criteria:

* The selected patients has a badly decayed mandibular posterior teeth which are indicated for extraction due to dental causes (periapical abscess, trauma or caries) not periodontal as diagnosed by periapical x-ray.
* Healthy patients who are classified according to the American Society of Anesthesiologists (ASA)(2022) physical status classification as class I.
* Patient age ≥ 20 years old.
* Surgical site with sufficient for implant placement.
* Sufficient interocclusal space for prosthesis.
* Good oral hygiene.
* Patients have thick biotype.
* Patients have socket class I.

Exclusion Criteria:

* Active periodontal diseases and periapical lesions not chronic infections.
* Patients have parafunctional
* History of alcohol or drug dependency, psychological factor that might affect the surgical or prosthodontic treatment.
* Smoking.
* Pregnant patients.
* Patients who are not willing to complete the study.

+Locations (1)

FacilityCityCountryStatus
Delta University For Science And TechnologyAl MansurahEgypt

+Study documents