PRF plus corticosteroids vs PRF alone vs standard care for impacted lower wisdom teeth
Official title: Comparison of Postoperative Effects of PRF and Corticosteroid Treatments in Impacted Third Molar Surgery
Run by Final International University · NCT07742826 · Data updated 2026-11-12
This study tests whether using platelet-rich fibrin, with or without a corticosteroid, can reduce pain and swelling after removing an impacted lower third molar.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Final International University Academic / other |
| Locations | 1 site (Nicosia) |
| Status | Recruiting |
| Started | September 3, 2024 |
| Main results expected | August 2026 |
| Study ends | August 2026 |
| Registry record updated | August 3, 2026 |
| Trial ID | NCT07742826 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 or older in good general health undergoing planned surgical extraction of an impacted mandibular third molar.
✕Probably not a fit
Patients with systemic diseases affecting healing, infection at the site, or contraindications to corticosteroids or study medications may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this randomized trial, 60 adults undergoing impacted mandibular third molar extraction are assigned to three groups: standard treatment, PRF alone, and PRF combined with corticosteroid. Postoperative outcomes—pain, facial swelling, and limited mouth opening—are measured on days 1, 2, 3, and 7 after surgery. The goal is to determine if PRF and/or its combination with corticosteroids improve recovery compared with standard care. The study uses typical postoperative medications and oral hygiene measures as part of routine care. Results may influence postoperative management for impacted third molar extractions.
Why it matters
Potential benefit: If successful, participants receiving PRF, with or without corticosteroids, may experience less pain and swelling after surgery.
How similar studies have gone: Previous research suggests PRF and corticosteroids can influence healing and inflammation, but findings vary across settings.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 18 years and older. * Patients with good general health * Patients with complete clinical and radiographic examination (panoramic radiograph/CBCT if applicable) * Patients willing and able to attend all postoperative follow-up visits Exclusion Criteria: * Patients with systemic diseases that may impair wound healing (e.g., uncontrolled diabetes, immunodeficiency). * Pregnant or breastfeeding women. * Patients with acute infection, abscess, or pericoronitis at the surgical site. * Patients with a history of allergy or contraindication to corticosteroids, local anesthetics, or prescribed medications. * Patients using corticosteroids, anticoagulants, immunosuppressive drugs, or bisphosphonates. * Patients with bleeding disorders. * Patients with previous radiotherapy to the head and neck region. * Patients unable or unwilling to comply with the study protocol or attend follow-up visits.
Where it's running
-
Final International University Faculty of Dentistry
Nicosia, Cyprus Recruiting
Study contacts
- Study coordinator: Meliz Kneebone, DDS
- Email: meliz-95@hotmail.com
- Phone: +905338425731
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This trial will test whether four flap closure methods—traditional sutures, leaving the wound open, a small surgical drain, or a cyanoacrylate tissue adhesive—reduce pain, swelling, limited mouth opening, and improve recovery for healthy adults (18–40) having an impacted lower third molar removed.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.