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临床试验/CTRI/2020/05/025110
CTRI/2020/05/025110已完成1 期

Comparison of anesthetic efficacy of Ropivacaine and Lignocaine in patients with irreversible pulpitis: A double-blind randomized clinical trial.

SThendral0 个研究点目标入组 67 人开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
67

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

  • . Subjects with age range between 18 to 50 years.
  • 2. Subjects who were currently experiencing active pain in mandibular molars.
  • 3. Subjects without any systemic conditions.
  • 4. Participants should not be under any medications that would alter pain perception and
  • 5.The subjects should be clinically diagnosed with irreversible pulpitis, determined by spontaneous pain and prolonged response to cold testing with Endofrost (Coltene-Roeko) and a positive response to electric pulp testing, with absence of any periapical radiolucency on radiographs except for a mild widening of periodontal ligament space and a vital coronal pulp on access opening.
  • 6. Every subject had atleast one opposing or contralateral molar without any deep coronal restoration, extensive caries, periodontal disease, which was used as a control while pulp testing.

排除标准

  • . Patients with systemic conditions,
  • 2. Pregnant and Lactating women,
  • 3. Mandibular molars with periapical radiolucency,
  • 4. Mandibular molars without vital pulp tissue were later excluded during endodontic procedures

研究者

发起方
SThendral

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