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临床试验/NCT06457828
NCT06457828招募中不适用

Effect of Apical Patency and Local Corticosteroid on Pain and Neuropeptides Release in Patients With Symptomatic Irreversible Pulpitis: A Randomized Clinical Trial

Suez Canal University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年2月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Inflammatory markers

研究概览

简要总结

The goal of this randomized clinical trial is to learn the effect of using local corticosteroids and maintaining apical patency in reducing post-preparation pain in patients with acute irreversible pulpitis in molar teeth. The main question it aims to answer is:

• How effective are using local corticosteroids and maintaining apical patency in reducing post-preparation pain in patients with acute irreversible pulpitis? Participants will be asked to fill a visual analogue scale to record their pain, after receiving a root canal treatment while using local corticosteroids or not as well as maintaining apical patency or not.

Researchers will compare the use of corticosteroids and maintaining apical patency in reducing post-operative pain.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
21 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Symptomatic acute irreversible pulpitis in molar teeth.
  • Normal periapical condition including periapical radiography with minimal widening of periodontal ligament.
  • Normal probing depth.
  • No medical condition.
  • No contraindication for administration of corticosteroids and local anesthesia.

排除标准

  • Facial or oral paresthesia.
  • Pregnancy & breastfeeding.
  • Unrestorable tooth.
  • Marginal periodontal disease.
  • Presence of a crown on the tooth involved.
  • Over instrumentation during root canal treatment.
  • Long-term use of corticosteroids.
  • False-positive cases of sensibility test with necrosis discovered after gaining access to the tooth.
  • Cases requiring intrapulpal injection to promote anesthesia.

研究组 & 干预措施

No apical patency

Sham Comparator

干预措施: Non-corticosteroid injection (Procedure)

No apical patency

Sham Comparator

干预措施: Corticosteroid injection (Drug)

Apical patency

Active Comparator

干预措施: Non-corticosteroid injection (Procedure)

Apical patency

Active Comparator

干预措施: Corticosteroid injection (Drug)

结局指标

主要结局

Inflammatory markers

时间窗: before treatment, after 3 days and after 7 days

Gingival crevicular fluid samples were collected by periopaper for testing the level of IL-1β and IL-10

Post-operative pain

时间窗: 6, 12, 24, 48, 72 hour and 7 days postoperative intervals

Patients were instructed to record their pain level using the Visual Analog Scale

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

Mustafa M. Sultan

Teaching assistant

Suez Canal University

研究点 (1)

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