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临床试验/NCT06021301
NCT06021301招募中2 期

Injectable Platelet-Rich Fibrin and Microneedling For Papillae Reconstruction In Esthetic Zone (A Case Series )

Cairo University1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2023年11月最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
10
试验地点
1
主要终点
Papillary height

研究概览

简要总结

The currently available non-surgical techniques for papillary reconstruction did not provide long term maintenance of papillary regeneration, Surgical techniques are invasive and the results are unpredictable . The study is based upon the positive effects of iPRF upon enhancing wound healing in terms of new collagen formation, angiogenesis and increasing keratinized tissue phenotype . iPRF exhibited comparable effects to subepithelial connective tissue graft in papillary reconstruction . The effect of microneedling on the tissue responds as if experiencing tissue trauma and the body's own collagen production is induced to preserve tissue integrity . Growth factors are released immediately after injury, inducing the proliferation of new cells, and fibroblasts are transformed into collagen and elastin fibres from day 5 up to week 8 .

详细描述

The patients diagnosed with black triangles according to Norland classification system for loss of papillary height will be selected. Each patient will receive a proper knowledge of the study protocols along with full-mouth scaling and root planing (SRP) using ultrasonic and hand instruments and will be given personalized oral hygiene instructions. After oral prophylaxis and baseline measurements of insufficient interdental papilla the treatment will be MN and iPRF. First, MN will be done in the required area with insulin syringe gauge 30,The interdental papilla will vertically and horizontally measured in mm. By establishing a ratio and proportion, the number of microchannels in the region to be treated will calculated to be 250 microchannels per square cm. Then, a venous blood sample will be taken for each patient using a 10-ml injector into i-PRF tube containing no anticoagulant and centrifuged at room temperature for 3 min at 700 rpm (60 g force). The 30-gauge dental injector needles will be used for injection of i-PRF. The needle will be inserted at 45° angle, 2-3-mm apical to the involved papilla and all surrounding areas will receive iPRF. Each involved papilla will be injected with an amount till blanching is visible . This method will be repeated for 4 times at 10 days intervals consecutively. The final clinical photographs and measurements will recorded 3 and 6 months of last dose administered . After the intervention, patients will receive oral hygiene instructions that include the roll technique when brushing without the use of floss and toothpick during the study period to minimize trauma to the treated site .

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Nonsmoking patients aged above 18 years.
  • At least one site with interdental papilla recession in the anterior region of the maxillary or mandibular jaws.
  • The distance from the contact point to alveolar bone is crest < 7 mm.
  • Class I or Class II papillary recession, according to Nordland and Tarnow's classification systems (Nordland et al., 1998).
  • No active periodontal diseases and good oral hygiene.

排除标准

  • Patients were excluded from the study if they have:
  • Spacing or crowding between the teeth to be treated
  • Abnormal tooth shape
  • Systemic diseases such as diabetes mellitus, hypertension or conditions that alter the outcome of periodontal therapy.
  • In addition, patients will be excluded if they are Pregnant and lactating women.

结局指标

主要结局

Papillary height

时间窗: at 3,6 months

using UNC probe from papillary tip till incisal edge.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yasmeen Saleh Tolba

Resident at Faculty of Oral and Dental medicine, Cairo University.

Cairo University

研究点 (1)

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