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临床试验/NCT04119661
NCT04119661已完成不适用

Postendodontic Pain on Using Max-i-Probe vs NaviTip as Irrigation Needles: A Randomized Clinical Trial

Cairo University0 个研究点目标入组 180 人开始时间: 2012年7月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
180
主要终点
Postoperative pain using a pain-measuring scale

研究概览

简要总结

The aim of this prospective, randomized, clinical trial was to evaluate the effect of the side-vented Max-i-Probe versus the end-vented NaviTip as endodontic needles during syringe irrigation on post-operative pain in adult patients with symptomatic irreversible pulpitis in posterior mandibular teeth.

详细描述

The aim of this prospective, randomized, clinical trial was to evaluate the effect of the side-vented Max-i-Probe versus the end-vented NaviTip as endodontic needles during syringe irrigation on post-operative pain in adult patients with symptomatic irreversible pulpitis in posterior mandibular teeth. Medical and dental history was obtained from all participants in this trial and clinical examination for teeth was performed. Participants with symptomatic irreversible pulpitis were included. After access cavity preparation, participants were randomly assigned to one of the following groups: experimental group (Max-i-Probe) or control group (NaviTip). One-visit root canal treatment was performed . Each patient received a 48-h diary to record postoperative pain. Post-operative pain was measured at the following time points: 4, 12, 24 and 48 hours after root canal treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
16 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: 16-65 year old.
  • Medically free.
  • Mandibular posterior teeth with symptomatic irreversible pulpitis.
  • No sex predilection

排除标准

  • Pregnant females.
  • History of allergy to any medication used in the study.
  • Preoperative premedication less than 6 hours before procedure.
  • Cracked teeth and teeth with badly-decayed crowns.

研究组 & 干预措施

Max-i-Probe

Experimental

干预措施: Max-i-Probe (Device)

NaviTip

Active Comparator

干预措施: NaviTip (Device)

结局指标

主要结局

Postoperative pain using a pain-measuring scale

时间窗: 48 hours

Postoperative pain is measured using the Numerical Rating Scale (NRS) which is an 11-point scale from 0-10 where 0 represents no pain and 10 represents the worst pain measured 48h after root canal treatment

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Suzan AW Amin

Professor

Cairo University

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