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NCT07652216Active, not recruiting

Bone Defects Reconstruction After Dentigerous Cyst Enucleation With Autogenous Demineralized Dentin Matrix- ADDM and Advanced Platelet-Rich Fibrin- A-PRF.

Source: ClinicalTrials.gov · Last updated 23 Jun 2026

Brief summary (registry, in English)

This prospective clinical study evaluates bone healing following dentigerous cyst enucleation associated with impacted mandibular third molar extraction. The study compares spontaneous blood clot healing, Advanced Platelet-Rich fibrin (A-PRF), and A-PRF combined with Autogenous Dentin Demineralized Matrix (ADDM). Bone healing is assessed as the primary outcome, while postoperative pain intensity assessed using the Numerical Rating Scale (NRS) with graphical representation represents a secondary outcome. The study aims to determine whether the use of A-PRF or A-PRF combined with ADDM improves postoperative healing outcomes compared with spontaneous blood clot healing.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
35 (actual)
First submitted
11 Jun 2026
Start date
4 Apr 2024
Primary completion date
1 Dec 2026
Lead sponsor
Jagiellonian University
NCT number
NCT07652216

What you commit to

  • Study type: Interventional
  • Participants enrolled: 35
  • From 4 Apr 2024 to the primary completion date, 1 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Immunosuppressive therapy
  • Use of medications affecting bone metabolism

Other illness

  • Acute local infection at the surgical site
  • Systemic diseases affecting bone healing or tissue regeneration
  • History of radiotherapy in the head and neck region

Lab values

  • Hematological disorders affecting platelet function, coagulation, or fibrin formation (including thrombocytopenia, coagulopathies, or anticoagulant therapy).

Other

  • Pregnancy or breastfeeding
  • Heavy smoking
  • Inability to comply with follow-up visits or postoperative recommendations

Who the study is looking for

  • Patients diagnosed with dentigerous cysts associated with impacted mandibular third molars
  • Indication for surgical enucleation and tooth extraction
  • Ability to provide informed consent
  • Availability for postoperative follow-up examinations and CBCT assessment

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Oral Surgery, Institute of Dentistry, Jagiellonian University Medical College
Coordinator of this site? Confirm its status
KrakowPolandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.