Comparing two types of platelet-rich fibrin for dental implants

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to compare the effectiveness of two different types of platelet-rich fibrin (Alb-PRF and L-PRF) when used in conjunction with xenograft for immediate dental implant placement. It will evaluate various parameters such as peri-implant vertical defect depth, crestal bone level, bucco-lingual bone width, and keratinized tissue width. The study will involve patients with non-restorable mandibular molars who meet specific inclusion criteria and will assess the outcomes of the implants placed using these two different fibrin preparations.

Why it matters

Who can join: the full rules

1. Inclusion criteria

   * The presence of non-restorable mandibular molar.
   * Patient 18-45 years old
   * Intact buccal and lingual walls
   * Good oral hygiene.
   * Prescence of sufficient restorative space.
   * Jumping gap more than 2 mm.
2. Exclusion criteria

   * Proximity of anatomical structures
   * Acute localized infection (suppuration at the surgical field)
   * Patients on chemotherapy or radiotherapy.
   * Patients who have systemic disorders (diseases) {diabetes mellitus, autoimmune disease, …etc},
   * Pregnant patients.
   * Smoking and Alcohols.
   * Presence of periapical pathology affecting the neighboring teeth.

Where it's running

• Kafrelsheikh University, Faculty of Dentistry
  Kafr ash Shaykh, Kafrelsheikh, Egypt Recruiting

Study contacts

• Study coordinator: Mostafa Mohamed Fayed, Demonstrator of Periodontology
• Email: mostafa.mohamed@den.kfs.edu.eg
• Phone: 0201004668099

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.