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临床试验/NCT01561183
NCT01561183已完成不适用

Vital Pulp Therapy for Management of Irreversible Pulpitis in Human Permanent Teeth: A Randomized Clinical Trial.

Shahid Beheshti University of Medical Sciences1 个研究点 分布在 1 个国家目标入组 302 人开始时间: 2012年3月1日最近更新:
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
302
试验地点
1
主要终点
Clinical and radiographical success rates (%) of each treatment group

研究概览

简要总结

To compare the effect of different VPT methods using Calcium Enriched Mixture (CEM) cement for management of human dental pulp with irreversible pulpitis.

详细描述

The purpose of this randomized clinical trial is to demonstrate the effect of four methods of Vital Pulp Therapy (VPT) using a new endodontic bio-material [calcium enriched mixture (CEM) cement] in pain relief as well as clinical/radiographic success, for management of irreversible pulpitis of human permanent teeth.

研究设计

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

入排标准

年龄范围
10 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Carious permanent vital mature molar tooth with closed apex (with preoperative X-ray)
  • •Positive response to EPT or cold test
  • •patients willing to participate in study
  • •Healthy subjects; absence of any systematic disorder
  • •Age ≥ 10 years old
  • •Both gender
  • •Written informed consent

排除标准

  • •Moderate or severe periodontitis; pockets >3mm
  • •None restorable tooth
  • •Internal or external root resorption
  • •Root canal calcification
  • •Non vital pulps
  • •Analgesic taken within the last 8h
  • •Active systemic disease
  • •Pregnancy or nursing
  • •History of opioid addiction/abuse
  • •Temporary residency

研究组 & 干预措施

Indirect pulp capping (IPC)

Experimental

Indirect pulp capping

干预措施: Indirect pulp capping (IPC) (Procedure)

Direct pulp capping (DPC)

Experimental

Direct pulp capping

干预措施: Direct pulp capping (DPC) (Procedure)

Miniature pulpotomy (MP)

Experimental

Miniature pulpotomy

干预措施: Miniature pulpotomy (MP) (Procedure)

Full pulpotomy (FP)

Experimental

Full pulpotomy

干预措施: Full pulpotomy (FP) (Procedure)

结局指标

主要结局

Clinical and radiographical success rates (%) of each treatment group

时间窗: 1 year

The outcome of clinical success/failure is determined by subjective symptoms and objective observation of inflammation/infection. The outcome of radiographic success is classified by using a modification of the Strindberg criteria.

次要结局

  • Patient Assessment of Pain with questionnaire(6-months)

研究者

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

Saeed Asgary

Dean of ICER

Shahid Beheshti University of Medical Sciences

研究点 (1)

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