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临床试验/NCT05876520
NCT05876520招募中不适用

Clinical and Radiographic Assessment of Nano-Bioactive Glass Combined With I-PRF Scaffold in Vital Pulp Treatments in Mandibular Molars With Closed Apices: A Triple Blinded "Randomized Controlled Trial"

Cairo University1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2023年1月25日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
28
试验地点
1
主要终点
Clinical , Radiographic and Success rate

研究概览

简要总结

Clinical, Radiographic and pain assessment of Vital pulp treatment in patients suffering from irreversible pulpitis in mature permanent molars. Total pulpotomy is investigated using I-prf only vs I-prf mixed with Nano-bioactive glass.

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

年龄范围
14 Years 至 32 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients suffering from Symptomatic irreversible pulpitis in mature mandibular molars only will be involved.
  • Tooth should give positive response to cold test
  • Haemostasias should be achieved after total pulpotomy
  • The tooth is restorable and free from advanced periodontal disease, cracks and splits.
  • Patients should be free from any systemic disease that may affect normal healing and predictable outcome.
  • Patients who will agree to the consent and will commit to follow-up period.
  • Patients with mature root apices
  • Patients with no internal or external resorption and no periapical lesions
  • Soft tissues around the tooth are normal with no swelling or sinus tract.

排除标准

  • Patients with immature roots.
  • Haemostasias after 10 minutes can not be controlled after total pulpotomy
  • Patients with any systemic disease that may affect normal healing.
  • Patients with periapical lesions or infections.
  • Pregnant females.
  • Patients who could/would not participate in a 6 months follow-up.
  • Patients with fistula or swelling
  • Patients with necrotic pulp.
  • Patients with old age.

结局指标

主要结局

Clinical , Radiographic and Success rate

时间窗: 6 month follow up

Presence or absence of clinical signs and symptoms + Radiographic periapical assessment + success rate based on Radiographic findings

次要结局

  • Pain intensity(Within the first 24 hrs upto the 7th day)

研究者

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

Noor Mohammed Kamal Eldeen Ahmed Mohmammed Sayed

Resident of Endodontics

Cairo University

研究点 (1)

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