Immediate Implant Placement With Subepithelial Connective Tissue Grafting and Probiotics

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-45
SponsorKafrelsheikh University

About this trial

The present study aims to evaluate and compare the clinical, radiographic, and biological peri-implant tissue outcomes of platelet-rich fibrin versus probiotics as adjuncts to immediate implant placement combined with subepithelial connective tissue grafting in adults requiring single immediate implant placement.

Eligibility criteria

Qualifiers

Adults aged 20 to 45 years.

Systemically healthy patients eligible for implant surgery.

Patients requiring extraction of a single non-restorable tooth indicated for immediate implant placement.

Implant sites located in the maxillary esthetic or para-esthetic zone.

Disqualifiers

Medically compromised patients or patients with systemic conditions that may contraindicate implant surgery or interfere with healing.

Smokers.

Pregnant or lactating women.

Patients with uncontrolled periodontal disease or poor oral hygiene.

Trial design

Treatments tested in this trial

  • Platelet-Rich Fibrin
  • Probiotics

Treatment groups

22 Participants
are divided into 2 treatment groups

Sponsors and collaborators