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临床试验/NCT05041738
NCT05041738Unknown不适用

Comparative Evaluation of the Efficacy of Intraoral Cryotherapy Versus Intracanal Cryotherapy on Postoperative Pain in Lower Molar Teeth With Irreversible Pulpitis and Symptomatic Apical Periodontitis Randomized Clinical Trial

Cairo University0 个研究点目标入组 68 人开始时间: 2021年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
68
主要终点
Postoperative pain assessed using Visual Analogue scale

研究概览

简要总结

The aim of this study is to clinically compare the efficacy of intraoral cryotherapy versus intracanal cryotherapy after single visit root canal therapy in lower molars with irreversible pulpitis and symptomatic apical periodontitis

研究设计

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

入排标准

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

入选标准

  • •Systemically healthy patient (ASA I or II).
  • •Mandibular first molar teeth with:
  • •Preoperative sharp pain and symptomatic apical periodontitis
  • •Absence or slight widening in the periodontal ligament (PDL).
  • •Vital response of pulp tissue to cold pulp tester (ethyl chloride spray) .
  • •Positive response to percussion test

排除标准

  • •Medically compromised patients.
  • •Pregnant women.
  • •Patients reporting bruxism or clenching.
  • •Patients allergic to ciprofloxacin or metronidazole.
  • •Teeth associated with acute periapical abscess and/or swelling.
  • •Greater than grade I mobility or pocket depth greater than 5mm.
  • •Size of periapical radiolucency is greater than 8 mm.
  • •No restorability: Hopeless tooth.
  • •Immature teeth.
  • •Radiographic evidence of external or internal root resorption vertical root fracture, perforation, calcification.

研究组 & 干预措施

Intraoral Cryotherapy

Experimental

干预措施: Intraoral Cryotherapy (Procedure)

Intracanal Cryotherapy

Active Comparator

干预措施: Intracanal Cryotherapy (Procedure)

结局指标

主要结局

Postoperative pain assessed using Visual Analogue scale

时间窗: 24 hours post treatment

Intensity of pain after root canal treatment will be recorded by the patient where "0= no pain, 1-3= mild pain, 4-6= moderate pain, 7-10= severe pain."

Postoperative pain assessed using Visual Analogue scale

时间窗: 6 hours post treatment

Intensity of pain after root canal treatment will be recorded by the patient where "0= no pain, 1-3= mild pain, 4-6= moderate pain, 7-10= severe pain."

Postoperative pain assessed using Visual Analogue scale

时间窗: 12 hours post treatment

Intensity of pain after root canal treatment will be recorded by the patient where "0= no pain, 1-3= mild pain, 4-6= moderate pain, 7-10= severe pain."

次要结局

  • Postoperative pain assessed using Visual Analogue scale(72 hours post treatment)
  • Postoperative pain assessed using Visual Analogue scale(48 hours post treatment)

研究者

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

Toka Mohamed Ezzat Kamel Soliman

Principal investigator, Resident at faculty of dentistry, Cairo University

Cairo University

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