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临床试验/CTRI/2021/02/031577
CTRI/2021/02/031577尚未招募未知

Determination of anesthetic efficacy of lidocaine alone and with magnesium sulphate, dexamethasone and ketorolac as adjuvants in symptomatic irreversible pulpitis -A randomized, double Blind Study.

Dr K Shekhar0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Age range of 18-60 years.
  • 2.Systemically healthy patients (ASA I /II).
  • 3.Patients who required endodontic treatment in lower teeth.
  • 4.Vital teeth with no history of root canal therapy.
  • 5.Patients who had tooth with clinical diagnosis of irreversible pulpitis.
  • 6.Volunteers who suffered from moderate or severe pain.
  • 7.Volunteers who signed a human subject committee approved consent form

排除标准

  • 1.Pregnancy or lactation patients.
  • 2.Patients who had taken analgesic or anti-inflammatory drugs within last 8hr.
  • 3.No volunteer under 18 years of age.
  • 4.Any endocrine or infections disease or had any systemic disease that contraindicate endodontic therapy.
  • 5.Active site of pathosis in the area of injection.
  • 6.Moderate to advanced periodontal disease.
  • 7.Non vital teeth (necrosis).
  • 8.Any known sensitivity or other adverse reactions to any of the medication or materials used in the study.

研究者

发起方
Dr K Shekhar

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