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临床试验/CTRI/2024/11/076805
CTRI/2024/11/076805招募中3 期

Comparative Evaluation of effect of Various Transdermal Patches and Oral NSAID on Post-Operative Endodontic Pain and Quality of Life - A Randomized Controlled Trial

Dr Balaram A1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2024年11月25日最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
200
试验地点
1
主要终点
Post Operative Pain relief

研究概览

简要总结

Post-operative pain occurs only in 25-40 % patients and can last up to several days, depending upon peripheral and central mechanisms of hyperalgesia. Pulpal inflammation and necrosis with the corresponding peri radicular tissue changes cause the release of inflammatory mediators, including prostaglandins which are involved in pain medication. The rationale for the pharmacological management of post-endodontic pain is focused on the reduction of chemical inflammatory mediators that activate or sensitize peripheral nociceptors and the subsequent events involved in pain perception. Prostaglandin suppression is important as it lowers the pain threshold (i.e. allodynia) and sensitizes nociceptors to other pain mediators. Ibuprofen is the most frequently used NSAID for control of pain associated with root canal treatment. This trial will compare the efficacy of transdermal and oral analgesic delivery systems in managing post-operative endodontic pain.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Systemically Healthy Individuals with symptomatic irreversible pulpitis and apical periodontitis.

排除标准

  • Systemic Disease Pregnancy Lactation PA Abscess Drug Allergies Analgesic intake within last 24 hours.

结局指标

主要结局

Post Operative Pain relief

时间窗: 0 hours, 12 hours , 24 hours , 48 hours and 72 hours

次要结局

  • Quality of Life Assessment(2 weeks)

研究者

发起方
Dr Balaram A
申办方类型
Other [Self Funded]
责任方
Principal Investigator
主要研究者

Dr A Balaram

Meenakshi Ammal Dental College and Hospital

研究点 (1)

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