ClinicalTrials.gg
CompletedNCT07841301Updated Sep 25, 2026

PRF Versus Emdogain for Class II Furcation Defects of Mandibular Molars

An interventional study of Platelet rich fibrin and Emdogain in Peridontal Disease and Furcation Defects, sponsored by Medical University of Sofia. Completed at 1 site in Bulgaria. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-25.

Sponsored by Medical University of Sofia · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 years 9 months after the study started (first participant enrolled Dec 2021, registered Sep 2026).
Updated Sep 25, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
21
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This study evaluated the regenerative potential of platelet-rich fibrin (PRF) compared with enamel matrix derivative (Emdogain®) in the surgical treatment of Class II (F2) furcation defects of mandibular molars. Twenty-one systemically healthy patients with a total of 30 mandibular molars presenting with buccal Class II furcation defects were included. The furcation defects were treated surgically with either PRF or Emdogain®. Clinical parameters, including periodontal probing depth, clinical attachment level, bleeding on probing, and furcation involvement, were assessed before treatment and during follow-up. Clinical and radiographic measurements of the furcation defects were also performed. The main follow-up evaluation was conducted 6 months after surgery. The study compared the clinical and radiographic outcomes of PRF and Emdogain® in the treatment of mandibular molars with Class II furcation defects.

02

Conditions studied

  • Peridontal Disease
  • Furcation Defects

Keywords

  • Periodontitis
  • Class II furcation defects
  • Platelet-rich fibrin
  • Emdogain
  • Periodontal regeneration
  • Mandibular molars
03

In context

Furcation Defects

42 studies on the registry are indexed under Furcation Defects; 13 are open to participants now.

This study's enrollment of 21 is below the median of 27 across 38 interventional studies indexed under Furcation Defects.

Browse Furcation Defects studies →

Lead sponsor

Medical University of Sofia is the lead sponsor of 12 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Systemically healthy individuals
  • Stage III or Stage IV periodontitis
  • without allergies.

Exclusion criteria

Exclusion Criteria:

  • Smoking
  • Inadequate plaque control
  • Systemic diseases that may compromise periodontal therapy, including diabetes, immunodeficiency, or viral diseases.
  • therapy.
  • Treatment with bisphosphonates.
  • Treatment with anticoagulants.
  • Treatment with antiplatelet agents.
  • Thrombocytopenia.
  • Hypofibrinogenemia.
  • Hemophilia.
  • Other coagulation disorders.
  • Pregnancy.
  • Breastfeeding.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
21 participants (actual)

Study arms

  • Experimental
    PRF

    Surgical treatment of a mandibular molar with a Class II (F2) furcation defect using platelet-rich fibrin (PRF) following surgical debridement and root surface instrumentation.

    Biological: Platelet rich fibrin

  • Active comparator
    Emdogain

    Surgical treatment of a mandibular molar with a Class II (F2) furcation defect using enamel matrix derivative (Emdogain®) following surgical debridement and conditioning of the root surface with PrefGel®.

    Biological: Emdogain

Interventions

  • Surgical treatment of a buccal Class II furcation defect was performed under local anesthesia. Following flap elevation, complete instrumentation of the root surfaces and furcation defect was performed using hand and powered instruments (scaling and root planing). Horizontal and vertical furcation involvement were measured. For PRF preparation, peripheral venous blood was collected into two vacuum tubes using a closed butterfly system. The tubes were centrifuged using a PRF DUO centrifuge. PRF from one tube was used to fill the furcation defect, while PRF from the second tube was compressed to form a membrane covering the furcation entrance. The flap was coronally positioned and secured with sling and interrupted interdental sutures using resorbable 6-0 sutures.

    Also known as: PRF

  • BiologicalEmdogain

    Surgical treatment of a buccal Class II furcation defect was performed under local anesthesia. Following flap elevation, complete instrumentation of the root surfaces and furcation defect was performed using hand and powered instruments (scaling and root planing). Horizontal and vertical furcation involvement were measured. The exposed root surfaces were conditioned with 24% EDTA gel (PrefGel®, Straumann; pH 6.7) for 2 minutes, followed by thorough irrigation with sterile saline. Enamel matrix derivative (Emdogain®) was then immediately applied, starting from the most distant part of the furcation defect and covering the entire exposed root surface. The flap was coronally positioned and secured with sling and interrupted interdental sutures using resorbable 6-0 sutures.

    Also known as: enamel matrix proteins

06

What researchers measure

Primary outcomes

  1. Change in Horizontal Furcation Probing Depth

    Change in the horizontal probing depth of the furcation defect, measured at the furcation entrance before surgery and 6 months after surgery. The measurement was used to assess the horizontal component of furcation involvement and the clinical response to treatment.

    Time frame: Baseline to 6 months after surgery

Secondary outcomes

  1. Change in Probing Pocket Depth

    Change in periodontal probing depth at the treated furcation site, measured from m.gingivalis to the bottom of the pocket.

    Time frame: Baseline to 6 months after surgery

  2. Change in Clinical Attachment Level

    Change in clinical attachment level at the treated furcation site, measured from cementoenamel junction to the bottom of the pocket.

    Time frame: Baseline to 6 months after surgery

  3. Change in Vertical Bone Loss

    Change in vertical bone loss associated with the furcation defect, measured on three-dimensional imaging.

    Time frame: Baseline to 6 months after surgery

  4. Change in Horizontal Bone Loss.

    Change in horizontal bone loss associated with the furcation defect, measured on three-dimensional imaging.

    Time frame: Baseline to 6 months after surgery

07

Study locations

1 site
  • Department of Periodontology, Faculty of Dental Medicine, Medical University of Sofia
    Sofia, Bulgaria
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Dec 2021 to primary completion in May 2023, 17 months.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 19, 2026
First posted
Sep 25, 2026
StartActual
Dec 2, 2021
Primary completionActual
May 29, 2023
CompletionActual
May 29, 2023
Last update
Sep 25, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Sep 25, 2026
Show all 1 update
  1. Sep 25, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07841301
Lead sponsor
Medical University of Sofia
Responsible party
Sponsor
First posted
Sep 25, 2026
Start date
Dec 2, 2021
Primary completion
May 29, 2023
Completion
May 29, 2023
Last update
Sep 25, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: P-prf

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