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临床试验/ISRCTN14290358
ISRCTN14290358已完成不适用

Assessment of the procedure duration and efficacy of pulpotomy and partial pulpectomy in comparison with total pulpectomy for patients with symptomatic irreversible pulpitis: a randomized clinical trial

Baskent University0 个研究点目标入组 66 人开始时间: 2017年6月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
66

研究概览

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Aged between 18 and 60 years
  • 2. Male or female
  • 2. Acute dental pain in posterior maxillary or mandibular molar teeth
  • 4. Diagnosed with symptomatic irreversible pulpitis with or without symptomatic apical periodontitis

排除标准

  • 1. History of American Society of Anesthesiologists (1963) III-VI status
  • 2. Pregnancy or nursing
  • 3. Mental disability
  • 4. History of allergy to nonsteroidal anti-inflammatory drugs, and analgesic treatment during the 12 hours prior to presentation
  • 5. If the subject tooth has moderate or severe marginal periodontitis, horizontal or vertical fractures, internal or external root resorption, root canal calcification, or a nonrestorable crown defect
  • 6. If an opposing and/or neighbouring tooth has defective restorations, deep caries, moderate or severe marginal periodontitis, wear, or history of recent tooth preparation.

研究者

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