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Periodontitis Stage IINCT07080294

Use of Injectable Extended Platelet-Rich Fibrin as a Local Drug Delivery in the Treatment of Stage II Periodontitis Patients

A study testing extended platelet rich fibrin injection in pocket, albumin injection in pocket and scaling and root planing in people with Periodontitis Stage II and Gingival Pocket, run by Mansoura University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The objective of the present study is to assess the clinical effectiveness of local delivery of injectable extended platelet-rich fibrin in subgingival application when used in conjunction with scaling and root planing (SRP) in the treatment of stage II periodontitis. Read more about this study

Who is it for?
Ages 30 to 50 years
Conditions the study is for
Periodontitis Stage II, Gingival Pocket
What is being tested?
extended platelet rich fibrin injection in pocket, albumin injection in pocket and scaling and root planing
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteEgypt
Study dates
17 Apr 2024to 17 Jun 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 30 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Patients with stage II Periodontitis (pocket depth ≤ 5mm and CAL = 3-4 mm).
  • Age range (30-50) years.
  • Good compliance with the plaque control instructions following initial therapy.
  • Availability for follow- up and maintenance program.

Who cannot join

  • Periodontitis patients with stage I, III and IV.
  • Smoking.
  • Systemic diseases which could influence the outcome of the therapy.
  • Pregnant and lactating females.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Mansoura university

    Al Mansurah, DK, 35516

Other trials in Egypt

About this study

Official title: Use of Injectable Extended Platelet-Rich Fibrin as a Local Adjunctive Therapy in the Treatment of Stage II Periodontitis Patients (Randomized Controlled Clinical Trial)

The objective of the present study is to assess the clinical effectiveness of local delivery of injectable extended platelet-rich fibrin in subgingival application when used in conjunction with scaling and root planing (SRP) in the treatment of stage II periodontitis.

The primary outcome includes the clinical attachment gain after 6 months, whereas the secondary outcomes include the changes of probing pocket depth, bleeding on probing percentage, plaque and gingival indices and the concentration of matrix metalloproteinase-8 (MMP-8) in gingival crevicular fluid (GCF) after 3 and 6 months.

Read the detailed description

Periodontitis is a chronic inflammatory dysbiotic disease resulting in damage of the periodontal tissue surrounding the teeth. At first, the teeth loosen, and eventually, there may be tooth loss. Periodontitis occurs due to an imbalance in the oral microbiota's natural balance and host resistance (i.e., dysbiosis). In adults, dysbiosis may be the cause of periodontitis, which can lead to inflammatory changes that affect the bone and connective tissue (1, 2).

The goals of today's treatment of periodontitis are to reduce infection, resolve inflammation and create a clinical condition, which is compatible with periodontal health (3). Periodontitis is typically treated initially in a non-surgical way. Non-surgical periodontal therapy consists of scaling and root planing (SRP) combined with oral hygiene instructions. Typically, this results in clinical attachment gain due to resolution of the inflammation. However, findings revealed that in some affected areas, the standard treatment proved to be insufficient and some residual pockets remain after therapy (4).

To reduce the indication of surgical invasive and technically demanding procedures, several adjuncts to SRP have been proposed such as the use of antibiotics or anti-inflammatory drugs. These adjunctive therapies improved treatment outcomes in terms of pocket depth reduction and CAL gain (5). However, their systemic administration requires the use of high dose of active drugs to reach efficient concentration at the treated site, the compliance of the patient to follow the selected administration regimen and could be associated with serious side effects. Consequently, several local treatments such as gels, fibers or chips loaded with different active molecules or drugs have been developed and evaluated in clinical settings (6).

The main advantages of such treatments are the delivery of active drugs at the precise site of the lesions, the reduced risk of side effects and the possibility of 3D stabilization of the blood clot (7). Local application of medications after scaling and root planing (SRP) has shown better results than SRP alone principally in reduction of pocket depth (8). Nonetheless, some materials which are applied locally were found to induce allergic -like reactions, lack the rheological characteristics and sustained release of the active ingredient under investigation (9).

To-date, platelet concentrates have been proven to promote and stimulate wound healing processes and to accelerate angiogenesis due to their concentrated growth factors content and anti-inflammatory molecules. Del Fabbro and his colleagues confirmed the use of growth factors for providing an additional stimulation to physiological healing processes (10).

Platelet concentrates are classified as platelet-rich plasma (PRP) or platelet-rich fibrin (PRF). In PRP techniques, blood is collected with anticoagulant and then centrifuged, whereas in PRF techniques, blood is collected without any anticoagulant and immediately centrifuged (11).

As for leukocyte- and platelet-rich fibrin (L-PRF) products, including L-PRF clots and liquid fibrinogen, platelet concentrates are obtained by centrifugation of a whole blood sample, discarding red blood cells and concentrating the components to be used, such as fibrin, platelets, growth factors, leukocytes, and other circulating cytokines and proteins (12). Nevertheless, the common demerit of current platelet concentrates is the fast resorption within 15 days inside the site of application (13).

Recently, a new PRF preparation has been introduced by Richard Miron (2020) known as extended platelet- rich fibrin (e-PRF) or Albumin-PRF mixture (Alb-PRF). It consists of a combination of concentrated growth factors and denaturated albumin gel. It is postulated that it might resorb after 4-6 months; therefore, it can be used even for guided bone regeneration (14) .

Extended platelet- rich fibrin (ePRF) is the latest functional and promising matrix that overcomes limitations of its predecessors. It shows many characteristics of ideal biomaterial for repair, regeneration, or facial esthetics. Here are some important characteristics: it is injectable which allows physicians to minimize access trauma to affected tissue and there is no need for sophisticated armamentarium for its production as a chairside procedure in the clinics (15).

ePRF can be used as a bioactive, natural filler as it forms a "sticky" gel that can be used as a 100% natural filler and it does not easily leak out from the injury site. Its gel creates a natural scaffold allowing absorption of water that is necessary for proliferation of new cells. It does not block the space for newly formed tissue (16).

Thus, the alternative hypothesis of the present study states that the injectable extended platelet rich fibrin could improve the periodontal status of patients who are suffering from stage II periodontitis.

Being tested
extended platelet rich fibrin injection in pocket, albumin injection in pocket, scaling and root planing
Keywords
eprf, periodontitis stage II, Alb prf, pocket, albumin, SRP, extended prf, extended platelet rich fibrin, gel
Medical subject headings
Periodontitis, Gingival Pocket

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • extended platelet rich fibrin injection in pocketOther

    Whole blood (10 mL) will be centrifuged at 700 g for 8 minutes. The upper layer (yellow layer) shows the liquid plasma layer. The most upper layer of platelet- poor plasma (PPP) will be collected in a syringe. then PPP will be heated in a heat block device at 75°C for 10 minutes and thereafter cooled to room temperature for approximately 2 minutes. An injectable albumin gel will then be prepared. Then the liquid platelet-rich layer (liquid-PRF) including the buffy coat layer with accumulated platelets and leukocytes, will be collected in a separate syringe. The albumin gel and native liquid PRF will then be thoroughly mixed by utilizing a female-female luer lock connector. Now injectable e-PRF in final form is ready to be used.

  • albumin injection in pocketOther

    Whole blood (10 mL) will be centrifuged at 700 g for 8 minutes. The upper layer (yellow layer) shows the liquid plasma layer. The most upper layer of platelet- poor plasma (PPP) will be collected in a syringe. then PPP will be heated in a heat block device at 75°C for 10 minutes and thereafter cooled to room temperature for approximately 2 minutes. An injectable albumin gel will then be prepared.

  • scaling and root planingOther

    removes plaque and calculus above and below the gumline using manual or ultrasonic instruments.

Study groups in NCT07080294
Study groupRoleWhat they receive
extended platelet rich fibrin injection in pocketExperimentalThorough periodontal mechanical debridement and injection of ePRF inside the assigned pockets will be performed for 15 patients of stage II periodontitis.
Receives: Other: extended platelet rich fibrin injection in pocket
albumin injection in pocketExperimentalScaling and root planing and injection of albumin gel alone inside the pockets will be performed for 15 patients of stage II periodontitis
Receives: Other: albumin injection in pocket
scaling and root planingExperimentalMechanical debridement alone will be performed for 15 patients with stage II periodontitis without injection of any material into the pockets.
Receives: Other: scaling and root planing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. clinical attachment gain

    Clinical Attachment Level (CAL) measured from the cementoenamel junction to the base of the gingival sulcus (RD+PD).

    Measured: 6 months

Secondary outcomes (4)
  1. Probing Depth (PD)

    The assessment of probing pocket depth involved measuring the distance from the free gingival margin to the base of the pocket using a 1 mm UNC 15 periodontal probe, which was inserted into the gingival sulcus parallel to the tooth's long axis. Readings were documented from three buccal sites-mesiobuccal, middle-buccal, and distobuccal-and three lingual sites-mesial-lingual, middle-lingual, and distal-lingual. The probing depths recorded (3-5 mm) were summed and divided by the total number of pockets to derive the mean probing pocket depth for each patient.

    Measured: 6 months

  2. Plaque index (PI).

    According to the Silness and Loe plaque index (1964), the cervical plaque level was determined by measuring soft deposit thickness, excluding coronal plaque extension. The scoring process utilized a UNC 15 periodontal probe (1 mm), dental mirrors, sharp explorers, and appropriate lighting, with an air jet applied to dry teeth and gingival tissues before evaluation.

    Measured: 6 months

  3. Gingival index

    The Löe and Silness index (1963) serves as a tool for examining gingival conditions by tracking qualitative changes. It evaluates the severity and spread of gingivitis, focusing on four designated sites per tooth, including the distofacial and mesiofacial papillae, the facial gingival margin, and the lingual gingival margin

    Measured: 6 months

  4. Bleeding on probing (BOP)

    A follow-up evaluation, the study further investigates bleeding on probing (BOP) as a clinical determinant of either periodontal disease progression or stability. The presence or absence of BOP is a well-established criterion for diagnosing periodontal health status.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jul 2025
  2. Study start17 Apr 2024
  3. Primary completion7 May 2025
  4. Study completion17 Jun 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07080294
Sponsor's protocol ID
A0401024OM
Status last verified
Jul 2025
First submitted
13 Jul 2025
Last updated
23 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing extended platelet rich fibrin injection in pocket, albumin injection in pocket and scaling and root planing in people with Periodontitis Stage II and Gingival Pocket, run by Mansoura University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

clinical attachment gain (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jul 2025.

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