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临床试验/PACTR202311897703701
PACTR202311897703701招募中Unknown

Postoperative pain control and quality of life following the use of preemptive celecoxib in mandibular third molar surgery

Stephen Solomon0 个研究点目标入组 62 人开始时间: 2023年9月24日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
62

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
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • 1.Patients within the age ranges of 18 to 50 years.
  • 2.Patients who shall be willing to keep instructions and follow-up appointments.
  • 3.Patients with mandibular third molar impaction requiring surgical extraction
  • 4.Patients who give their consent to be part of the study
  • 5.American Society of Anaesthesiologist physical status classification I (ASA I) patients

排除标准

  • 1.Patients with a history of allergy to celecoxib.
  • 2.Patients who are allergic to penicillins and metronidazole
  • 3.Patients who used NSAIDs or any other analgesic within 24 hours before the procedure
  • 4.Patients with a bleeding disorder or on anticoagulant
  • 5.Patients with peptic ulcer disease, kidney disease, asthma or any medical condition that contradict the use of NSAIDs.
  • 6.Pregnant women
  • 7.Patients with periapical cysts or tumours related to the impacted third molar
  • 8.Patients that could not be able to rate their pain intensity on the VAS due to medical conditions such as problems with vision, mental retardation, cognitive disorder, or any other reason.
  • 9.Patients who smoke, take alcohol or abuse drugs (illicit drugs)

研究者

发起方
Stephen Solomon

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