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临床试验/CTRI/2023/06/054464
CTRI/2023/06/054464尚未招募4 期

COMPARATIVE EVALUATION OF EFFICACY OF DICLOFENAC AND KETOPROFEN ADMINISTERED USING TRANSDERMAL DRUG DELIVERY ROUTE IN MANAGEMENT OF POST ENDODONTIC PAIN: A RANDOMIZED CONTROLLED CLINICAL TRAIL - NOT APPLICABLE

PANINEEYA INSTITUTE OF DENTAL SCIENCES0 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
4 期
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

  • i) Patients belonging to both sexes between the age group of 18 and 45
  • ii) Patients complaining of pain in single-rooted teeth of either jaw and
  • diagnosed as symptomatic irreversible pulpitis.
  • iii) Selected teeth should show intact lamina dura in intraoral periapical
  • radiograph with no periapical radiolucency and absence of
  • anatomical obstacles such as calcifications in the canals with no
  • anticipated procedural difficulties.
  • iv) Patients who give informed consent for the study

排除标准

  • i) Patients with hypersensitivity against diclofenac.
  • ii) Patients with a history of allergic reactions such as bronchospasm,
  • shock, urticarial, etc., following the use of diclofenac or other
  • non-steroidal anti-inflammatory drugs (NSAIDs).
  • iii) Patients with active stomach or duodenal ulceration within the last 6
  • iv) Patients undergoing treatment with other NSAIDs or corticosteroids
  • during the study period.
  • v) Patients with a history of systemic diseases such as bronchial
  • asthma, epilepsy, inflammatory bowel disease, severe liver or renal
  • insufficiency, dengue fever, emotional and psychosomatic
  • vi) Pregnant and lactating women.

研究者

发起方
PANINEEYA INSTITUTE OF DENTAL SCIENCES

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