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临床试验/IRCT201611242016N7
IRCT201611242016N7已完成未知

Compariosn of the combination of premedication with ibuprofen plus inferior alveolar block plus buccal infiltration with inferior alveolar block plus buccal infiltration on anesthesia success of posterior mandibular teeth with irreversible pulpitis: A three blinded randomized clinical trial

Vice Chancellor for Research and Technology0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
100

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

年龄范围
18 years 至 80 years(—)
性别
All

入选标准

  • Age 18 or more than 18 years, no contraindications to taking either Ibuprofen (history of any allergic reaction to aspirin, NSAIDS, or Lidocaine with Epinephrine, nasal polyp, history of peptic ulcers or GI bleeding, pregnancy and lactation, renal or hepatic disease), no history of GI disorders or ulcer, having no serious systemic disease.
  • Exclusion criteria: no response to cold test, having sensitivity to percussion and palpation, having radiographic changes such as PDL widening, lack of vital pulp in coronal pulp chamber access cavity preparation, teeth with evidence of crack in their crown, having advanced periodontal disease, taking narcotic drugs or analgesic drugs in recent 24 hours before treatment.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for Research and Technology

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