CompletedNot Applicable

Socket Preservation After Surgical Extraction of Impacted Lower Third Molar

Egypt45 participantsStarted 2022-12-01

Plain-language summary

The aim of this study will be to evaluate socket preservation using autogenous particulate dentin in combination with liquid platelet-rich fibrin versus bone allografts and collagen cone after surgical extraction of the horizontally impacted lower third molar

Who can participate

Age range18 Years – 35 Years

SexALL

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Inclusion criteria

✓. Fresh extracted socket of horizontally impacted mandibular third molar
✓. Co-operative patients willing to complete the follow-up periods.
✓. Patients age from 18-35 years.
✓. Good oral hygiene.

Exclusion criteria

✕. Any pathological condition at the site of surgery.
✕. Patients with systemic diseases that contra-indicate the surgical procedure such as uncontrolled diabetes mellitus, bleeding disorders, serious osseous disorders and mental disorders.
✕. Smokers .
✕. Pregnancy.

What they're measuring

bone resorption distal to second molar

Timeframe: 3 months after extraction

Trial details

NCT IDNCT06716736

SponsorWael Mohamed

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-12-15

View on ClinicalTrials.gov More Socket Preservation trials