About this trial
* The goal of study is to evaluate the effectiveness of adipose tissue derived-MSCs concentrate application in mandibular fractures. The main question it aims to answer is: Does intervention enhance bone quality, reduce complications and reduce bone regeneration time. * Researchers will compare the effectiveness of adipose tissue derived-MSCs concentrate application with ORIF to ORIF alone to see if MSCs improve healing in mandibular fractures. * Participants will:
* Be managed either by adipose tissue derived-MSCs concentrate application with ORIF or ORIF alone. * Undergo CBCT immediately (T1) and 3 months (T4) postoperatively for bone density radiographic evaluation * Visit the clinic postoperatively at one week (T2), one month (T3), three months (T4) for clinical examination
Eligibility criteria
Qualifiers
Patients with mandibular fracture.
Patients who are willing to participate in the study
Disqualifiers
Patients with systemic diseases influence bone healing
Patients with pathological fractures.
Infection located at the zone to be treated
Trial design
Treatments tested in this trial
- Adipose tissue derived mesenchymal stem cells concentrate application in addition to the open reduction and internal fixation.
- Open reduction and internal fixation