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临床试验/CTRI/2024/08/071805
CTRI/2024/08/071805尚未招募Unknown

Evaluating the pain at site, onset of action, duration and anesthetic efficacy of conventional, buffered lidocaine and precooled lidocaine with intraoral cryotherapy application in patients with symptomatic irreversible pulpitis: A clinical study. - NI

Shalini Reddy0 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
Unknown
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

  • diagnosed with Symptomatic Irreversible Pulpitis with moderate to severe pain (preoperative pain score=4) as measured on visual analog scale (VAS) participated in this trial. Criteria for inclusion were patients from 18 to 45 years of age and belonging to ASA category classes I and II with SIP in mandibular molar

排除标准

  • Patients who refused to give informed consent, allergic to local anaesthetics or any other drugs and/or conditions that influence the pain scores, and with presence of periapical radiolucency (other than a widened periodontal ligament), swelling, and sinus tract were excluded from the study.

研究者

发起方
Shalini Reddy

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