Evaluation of the safety and efficacy of PoroSyn, a synthetic bone graft in alveolar ridge augmentation - A single centre, open-label, randomized, comparative pilot study - PoroSyn Pilot Trial

SynThera Biomedical Private Limited0 个研究点目标入组 0 人开始时间: 待定最近更新: 2021年11月24日

试验速览

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•1. Need for tooth extraction
•2. Subject aged between 18-45 years of age belonging to either sex
•3. Non - smokers
•4. Presence of healthy adjacent teeth to the tooth to be extracted
•5. Medically fit and healthy patient, able to undergo oral surgical procedure under local anesthesia
•6. Subjects with good oral hygiene
•7.Able to sign Informed Consent

•-Patients requiring extraction of third molars
•-Acute infection or pus at the extraction site
•-Habits (Smoking, tobacco/ Beetle nut chewing)
•-Pregnant and lactating subjects
•-Presence of active periodontal disease
•-Subjects with poor oral hygiene and motivation
•-Subjects addicted to drugs or alcohol
•-Patients with psychiatric problem
•-Patients with condition affecting bone
•-Patients who are taking immunosuppressant medication
•-Patients who are taking anti-coagulant medication
•-Patients who have had or are undergoing radiation treatment of the graft region.
•-Patients with uncontrolled systemic diseases

发起方

SynThera Biomedical Private Limited