Efficacy Of Ibuprofen And Dexamethasone For Enhanced Success Of Inferior Alveolar Nerve Block In Irreversible Pulpitis: A Prospective, Randomized Clinical Trial
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
Chandani Agrawal
Dr. Ziauddin Ahmad Dental College and Hospital
