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临床试验/NCT06644703
NCT06644703已完成不适用

Effect of Cryotherapy on Postoperative Pain in Vital Pulp Treatment of Molar Teeth With Symptomatic Irreversible Pulpitis: A Randomized Controlled Trial

Cukurova University2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2023年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
62
试验地点
2
主要终点
Visual Analogue Scale

研究概览

简要总结

The goal of this clinical trial was to evaluate the effect of cryotherapy with salin solution on the intensity of postoperative pain after total pulpotomy procedures in molar teeth with symptomatic irreversible pulpitis. The main question it aims to answer is:

  • Does controlled irrigation with cold saline in total pulpotomy reduce the severity of postoperative pain? In the cryotherapy group, unlike the control group, after hemostasis was achieved, the coronal pulp cavity was irrigated with 2 °C saline solution for 5 minutes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

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

入选标准

  • moderate or severe pain
  • diagnosed with symptomatic irreversible pulpitis
  • no tenderness to percussion and palpation
  • positive response to cold test and electric pulp test
  • no signs of periapical pathology

排除标准

  • Teeth which
  • could not be restored or required post-core
  • had periapical lesions,
  • had poor periodontal status (pocket depth> 4 mm),
  • had negative responses to pulp sensitivity tests,
  • had no pulp exposure after caries removing Patients who
  • had no preoperative pain or had mild preoperative pain
  • had bleeding disorders
  • had systemic diseases such as immunosuppressive disease or diabetes

结局指标

主要结局

Visual Analogue Scale

时间窗: up to 72 hours

The visual analog scale for pain is a straight line with one end meaning no pain (0) and the other end meaning the worst pain (10) imaginable. A patient marks a point on the line that matches the amount of pain he or she feels. It may be used to help choose the right dose of pain medicine. Also called VAS.

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

Kübra Gürler

Cukurova University, Faculty of Dentistry

Cukurova University

研究点 (2)

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