跳至主要内容
临床试验/CTRI/2025/05/087007
CTRI/2025/05/087007尚未招募4 期

Efficacy Of Ibuprofen And Dexamethasone For Enhanced Success Of Inferior Alveolar Nerve Block In Irreversible Pulpitis: A Prospective, Randomized Clinical Trial

CHANDANI AGRAWAL1 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2025年5月20日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
600
试验地点
1
主要终点
pain assessment

研究概览

简要总结

Symptomatic irreversible pulpitis is a painful condition requiring root canal treatment, often characterized by heightened inflammatory mediator levels like prostaglandins (PGs) and leukotrienes. These mediators reduce the efficacy of local anesthetics, including inferior alveolar nerve block (IANB), by lowering the pain threshold and causing resistance to anesthesia. Non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and glucocorticoids like dexamethasone have shown promise in improving anesthetic outcomes by suppressing these mediators. Ibuprofen, at higher doses, has been effective in enhancing IANB success, while dexamethasone dual action on the COX and LOX pathways suggests its potential for similar benefits. However, limited research exists on the optimal dosages and combined effects of these drugs in improving anesthesia in cases of irreversible pulpitis. This study aims to evaluate the dose-dependent effects of ibuprofen and dexamethasone, individually and in combination, as oral premedications to enhance IANB success rates. It also seeks to identify the optimal dosages and assess the synergistic effects of these medications compared to a placebo, focusing on improving pain management during endodontic treatment.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • Patients experiencing moderate to severe pain and a prolonged response to pulp sensibility testing.
  • Should have a normal radiographic appearance.
  • 3.Should not have taken any analgesics for at least 12 hours before.
  • Systemically healthy patients.

排除标准

  • patients under 18 years old.
  • Patients with allergies and hypersensitivity to medications.
  • Pregnant or nursing women.
  • Immunocompromised patients.
  • Patients unable to give consent will be excluded from the study.

结局指标

主要结局

pain assessment

时间窗: pain assessment pre-operative, during access cavity, and during instrumentaion

次要结局

未报告次要终点

研究者

发起方
CHANDANI AGRAWAL
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Chandani Agrawal

Dr. Ziauddin Ahmad Dental College and Hospital

研究点 (1)

Loading locations...

相似试验