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临床试验/NCT06584188
NCT06584188尚未招募2 期

The Effect of Anti-inflammatory Cryoagent on the Level of Postoperative Pain in Patients With Symptomatic Irreversible Pulpitis and Apical Periodontitis.

Ain Shams University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年4月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Level of Post-operative pain.

研究概览

简要总结

  • The aim of this study is comparative between:
  1. Intra-radicular cryotherapy using cold anti-inflammatory {ketorolac tromethamine at 2-5C}.
  2. Intra-radicular final flush anti-inflammatory {ketorolac tromethamine at room temperature}.
  • In terms of:

C. Level of post-operative pain {POP} using a visual analog scale {VAS}. D. Level of substance P in periapical fluid will be analyzed by enzyme-linked immunosorbent assay (ELISA) kit.

Outcomes :

  • Primary outcomes: Level of Post-operative pain.
  • Secondary outcomes: Level of substance P expression

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients that will be diagnosed with symptomatic irreversible pulpitis and apical periodontitis.
  • Patient age ranging from 18-40 years.
  • Males or females.
  • Lower premolars.
  • Medically free patients.
  • Teeth with mature apex.
  • Teeth without any type of root resorption.

排除标准

  • Patients with other pulpal diagnosis.
  • Medically compromised patients.
  • Vulnerable group; pregnant females, mentally ill, etc...
  • Patients taking analgesics or anti-inflammatory drugs.
  • Teeth with open apex.

研究组 & 干预措施

Intra-radicular saline at room temperature

Experimental
  • Final flush with 20 mL of saline solution
  • At room temperature for 5 minutes.
  • Three samples will be collected from periapical fluid .

干预措施: anti-inflammatory ketorolac tromethamine (Drug)

结局指标

主要结局

Level of Post-operative pain.

时间窗: 48 hours post operative

measure intensity of post operative pain using visual analogue scale that was represented by a 100 mm horizontal ruler with no number markings other than a 0 at one end and a 10 at the other end. The following categories of postoperative pain levels were used to assess pain: 0 indicating no pain, mild pain (1-3), moderate pain (4-7) and severe pain (8-10)

Level of pre-operative pain.

时间窗: before start the operative

measure intensity of post operative pain using visual analogue scale that was represented by a 100 mm horizontal ruler with no number markings other than a 0 at one end and a 10 at the other end. The following categories of postoperative pain levels were used to assess pain: 0 indicating no pain, mild pain (1-3), moderate pain (4-7) and severe pain (8-10)

Level of Post-operative pain.

时间窗: 6 hours post operative

measure intensity of post operative pain using visual analogue scale that was represented by a 100 mm horizontal ruler with no number markings other than a 0 at one end and a 10 at the other end. The following categories of postoperative pain levels were used to assess pain: 0 indicating no pain, mild pain (1-3), moderate pain (4-7) and severe pain (8-10)

Level of Post-operative pain.

时间窗: 24 hours post operative

measure intensity of post operative pain using visual analogue scale that was represented by a 100 mm horizontal ruler with no number markings other than a 0 at one end and a 10 at the other end. The following categories of postoperative pain levels were used to assess pain: 0 indicating no pain, mild pain (1-3), moderate pain (4-7) and severe pain (8-10)

Level of Post-operative pain.

时间窗: 72 hours post operative

measure intensity of post operative pain using visual analogue scale that was represented by a 100 mm horizontal ruler with no number markings other than a 0 at one end and a 10 at the other end. The following categories of postoperative pain levels were used to assess pain: 0 indicating no pain, mild pain (1-3), moderate pain (4-7) and severe pain (8-10)

次要结局

  • Level of substance P expression.(Immediately prior to obturation)
  • Level of substance P expression.(15 minutes following access cavity preparation.)
  • Level of substance P expression.(30 minutes following access cavity preparation.)

研究者

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

abdulrahman ziad elwadiah

abdelrahman_ziad_kasem@dent.asu.edu.eg

Ain Shams University

研究点 (1)

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