牙科
牙槽嵴
牙本质
医学
口腔给药
放射性密度
透明质酸
核心活检
脱盐
山脊
软骨
试点试验
牙槽
软组织
生物活性玻璃
移植
植入
组织学
透明质酸钠
牙槽突
射线照相术
活检
作者
Hesham, Rahma,Shemais, Nesma,Saleh, Heba Ahmed,Fawzy El‐Sayed, Karim,Hesham, Rahma,Shemais, Nesma,Saleh, Heba Ahmed
摘要
ABSTRACT Objective The current trial assessed for the first time radiographic and histological alterations, following alveolar ridge preservation (ARP), using autogenous demineralized dentin graft carried in 0.2% high molecular weight sodium hyaluronate (ADDG+HA; test group) versus autogenous demineralized dentin graft (ADDG, control group) alone. Material and Methods Thirty patients ( n = 30) with non‐restorable single‐rooted teeth were randomly assigned into two groups ( n = 15/group). Following extraction, ARP was performed using either ADDG solely or ADDG+HA. Bucco‐lingual alveolar ridge width (BLRW; primary outcome), buccal (BRH) and lingual ridge height (LRH), percentage of newly formed bone, soft tissue and residual graft in human biopsies histologically, as well as patients' pain and discomfort (all secondary outcomes) were assessed after 6 months at the time of implant placement. Sample bone core biopsies were further collected, processed, and histomorphometrically and SEM analyzed. Results For the ADDG and ADDG+HA groups, the alveolar ridge dimensional changes were comparable, being −1.21 ± 0.77 mm and −1.18 ± 0.86 mm in BLRW, −0.89 ± 0.74 and −0.83 ± 0.85 mm in BRH, and −0.9 ± 0.76 mm and −1.05 ± 1.18 mm in LRH respectively ( p > 0.05). Clinically, no complications, pain, or inflammatory responses were reported. Histologically, all samples demonstrated bone growth and socket bone fill, while the ADDG+HA group showed a significantly greater presence of mineralized mature bone, which accounted for 33% ± 8.1% of the specimen after 6 months. Conclusions Both ADDG and ADDG+HA demonstrated comparable outcomes in terms of ARP. HA amalgamation with ADDG appears to enhance bone mineralization and maturation, yet without a significant impact on dimensional changes during ARP procedures. Trial Registration: NCT05613075
科研通智能强力驱动
Strongly Powered by AbleSci AI