Evaluating The Use of CGF Plugs in Fresh Odontectomy Socket.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-50
SponsorCairo University

About this trial

This study evaluates the use of Concentrated Growth Factor (CGF) plugs-a third-generation healing material made from the patient's own blood-to improve recovery after simple tooth extractions. CGF contains a dense matrix of growth factors and regenerative cells designed to enhance wound healing and tissue regeneration.

Participants requiring a single, non-surgical tooth extraction will have a CGF plug placed into the empty socket immediately following the procedure. The researchers will then monitor two main factors:

* Post-operative Pain: Patients will record their pain levels on a scale of 0 to 10 at 1, 3, and 7 days after the extraction. * Bone Density: Using specialized imaging (CBCT), the researchers will measure how well the bone heals and fills the socket immediately after the procedure and again at 3 months.

The goal of this research is to determine if CGF plugs can effectively reduce patient discomfort and help preserve bone density, which is critical for future dental treatments like implants.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Systemically healthy patients (ASA I or II)

Age between 20 and 50 years

Require simple, non-surgical extraction of a single tooth

Presence of periapical radiolucency at the extraction site

Disqualifiers

• Systemic diseases (e.g., uncontrolled diabetes, bone metabolic disorders)

History of radiotherapy or chemotherapy

Use of medications affecting bone metabolism (e.g., bisphosphonates, chronic steroids)

Heavy smokers

Trial design

Design model

Single group

Treatments tested in this trial

  • Concentrated Growth Factor (CGF) Plug

    Other intervention

    The intervention involves preparing an autologous Concentrated Growth Factor (CGF) plug from the patient's blood using variable-speed centrifugation and placing it into a fresh, curetted extraction socket to evaluate its impact on bone density and postoperative pain.

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: CGF Plug Intervention GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Bone Density

Evaluation of the extraction socket using Cone-beam computed tomography (CBCT) to assess changes in bone healing and preservation. Measurements are specifically analyzed and recorded using the Hounsfield unit scale to quantify mineral density within the site.

Time frame
Baseline assessment is conducted immediately after the tooth extraction and CGF plug placement, with a follow-up assessment performed at 3 months postoperatively.
2

Post Operative Pain

Clinical evaluation of pain using the Verbal Numeric Rating Scale (VNRS), where participants rate their pain on a scale from 0 to 10 (0 = No pain, 10 = Worst imaginable pain).

Time frame
Assessments are conducted at three specific intervals: Day 1, Day 3, and Day 7 following the surgical procedure.

Secondary outcomes

Other outcomes

Sponsors and contacts

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