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临床试验/NCT07738302
NCT07738302尚未招募不适用

Assessment of Post-Operative Pain After Using Cryotherapy and Dexamethasone in Symptomatic Irreversible Pulpitis With Acute Apical Periodontitis: A Randomized Clinical Trial.

Suez Canal University0 个研究点目标入组 60 人开始时间: 2026年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
主要终点
post-operative pain

研究概览

简要总结

Evaluation and comparing the effect of cryotherapy and dexamethasone on inflammatory mediators and post-operative pain in symptomatic irreversible pulpitis with acute apical periodontitis.

详细描述

sixty patients with single root teeth diagnosed with symptomatic irreversible pulpitis with acute apical periodontitis will be treated in two visits with time interval 72 hrs. Later, they will be randomized into four groups according to the type of irrigant used, group (A): (cold NaOCl , dexamethasone) for 1st visit and cold saline as final rinse for 2nd visit, group (B): ( NaOCl, dexamethasone) for 1st visit and saline as final rinse for 2nd visit (room temperature), group (C): cold NaOCl and cold saline and group D: NaOCl and saline room temperature as control group. Each group will be prepared with trunatomy rotary files according to manufactures instruction. Inflammatory mediators IL-8 and substance P will be assessed by absorbent paper points after access preparation and before obturation using ELISA test. Post-operative pain will be measured after first visit at 6,12, 24,48,72 hrs. then after second visit at 12,24,48,72hrs and 7 days using the visual analogue scale.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Medically free Patients. (ASA I and II)
  • Age between 20-50 years old.
  • Males & Females.
  • Patients' acceptance for participating in the trial through an informed consent (Appendix I)
  • Diagnosed clinically and radiographically with symptomatic irreversible pulpitis with apical peridontitits
  • No periapical radiolucency
  • Patent canals with n

排除标准

  • Non restorable teeth.
  • No bleeding upon conducting access preparation.
  • Teeth presenting with:
  • History of trauma or previous endodontic treatment

结局指标

主要结局

post-operative pain

时间窗: 7 days

VAS scale (visual analogue 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

Tamer Abdel Rahman Mahmoud

PhD candidate

Suez Canal University

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