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临床试验/ACTRN12619001349134
ACTRN12619001349134尚未招募2 期

The effectiveness of submucosal administration of methylprednisolone and dexamethasone in comparison to placebo after third molar surgery: a double blinded parallel arm randomized clinical trial

Dr Kinza Ayub0 个研究点目标入组 90 人开始时间: 2019年10月1日最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
20 Years 至 50 Years(—)
性别
All

入选标准

  • Patients in the age group – 20 to 50 years
  • Patients with mesioangular impactions Class II position B third molar according to the Pell and Gregory’s classification.
  • Patient with no medical conditions

排除标准

  • Patients requiring prophylactic antibiotics before surgical procedure. The following patients will be excluded because taking antibiotic before the treatment will subside the infection and pain and it will act as confounding factor with the study design
  • Patients suffering from any mental disorders or with any chronic pain problems. The following patients will be excluded because of ethical concerns.
  • Pregnant or lactating women. The following patients will be excluded to avoid any harm to pregnancy and fetus.
  • Patients reporting hypersensitivity to steroids. The following patients will be excluded because intervention includes application of steroids and they can have hypersensitivity or anaphylactic reaction
  • Patients taking nonsteroidal anti-inflammatory drugs in the 3 days before participation in the study. The following patients will be excluded because taking NSAIDS before the treatment will subside the infection and pain and it will act as confounding factor with the study design
  • Patients having acute pulpitis, abscesses, or other acute infections. The following patients will be excluded because of ethical concerns.
  • Patients with systemic disorders
  • Patients on long-term steroids

研究者

发起方
Dr Kinza Ayub

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