Socket type l and ll of Elian classification, anterior and premolar tooth Socket type l and ll of Elian classification Tooth derived bone graft materials Alveolar ridge preservation Palatal gingival graft Free gingival graft Allograft
Conditions
Interventions
Local anesthesia (4% articaine hydrochloride, Ubistesin 1:200,000
3M ESPE, Platz, Seefeld, Germany) was applied to the extraction sites. The tooth was then gently luxated with an elevator and carefully extracted using extraction forceps, with the intention of minimi
Ethicon, Norderstedt, Germany) were used. Bleeding at the palate was controlled by using a gauze pack or electrocautery. ,Local anesthesia (4% articaine hydrochloride, Ubistesin 1:200,000
Bangkok Material Center, Faculty of Medicine Siriraj Hospital, Bangkok, Thailand) until they were filled to a point 3 mm below the marginal bone, after which they were covered with a free gingival gra
Alveolar ridge preservation with dpDTM and FGG,Alveolar ridge preservation with FDBA and FGG,Alveolar ridge preservation with FGG
Sponsors
Ministry of Higher Education, Science, Research and Innovation, Prince of Songkla University
Eligibility
Sex/Gender
All
Age
20 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Adults patients (> 20 years old). 2.Residual extraction sockets of one upper or lower anterior and premolar tooth in Elian socket classification type l and ll. 2.The patient can sign the consent form to participate in the study and able to follow up on the appointment. 3.Presence of adjacent (mesial and/or distal) tooth at the extraction site. 4.Systemically healthy patients and cessation of smoking for 1 week before treatment. 5.No contraindication for minor oral surgery.
Exclusion criteria
Exclusion criteria: 1.Patients with a history of malignancy radiotherapy or chemotherapy for treatment of malignancy. 2.Pregnant patient or intending to become pregnant or nursing at the time of study inclusion. 3.Patients taking medications or having treatments with an effect on healing in general eg. steroids, large doses of anti-inflammatory drugs and bisphosphonates. 4.Patients have an active infection in the area of study. 5.Patients have severe periodontal disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Survival rate of free gingival graft Immediately, 3 days, 1 week, 2 weeks, 1 month Clinical photograph | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical volume of alveolar ridge Immediately, 1 and, 3 months after ARP cubic millimeter,Vertical alveolar bone alteration Immediately and 3 months after ARP millimeter,Horizontal alveolar bone alteration Immediately and 3 months after ARP millimeter,Mineralized tissue volume changes Immediately and 3 months after ARP cubic millimeter | — |
Countries
Thailand
Contacts
Public ContactSrisurang Suttapreyasri
Prince of Songkhla university
Outcome results
None listed