跳至主要内容
临床试验/NCT06506526
NCT06506526已完成不适用

Clinical, Radiographical and Microbiological Evaluation of Chitosan as Irrigating Solution for Pulpectomy in Non-Vital Primary Teeth

Suez Canal University1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2022年11月14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
45
试验地点
1
主要终点
Spontanous Pain

研究概览

简要总结

45 teeth will be sub-divided at random with a computerized method, according to the type irrigant and duration of its application into 3 groups (15 teeth in each group):

Group1(control group):

The teeth will be irrigated by 2 ml 1% NaOCl after each file.

Group2:

The teeth will be irrigated by 2 ml 1% NaOCl after each file then with 5 ml of 0.2% chitosan for one minute.

Group 3:

The teeth will be irrigated by 2 ml 1% NaOCl after each file then with 5 ml of 0.2% chitosan for 3 minutes.

Evaluation

Clinical evaluation will be done for all groups at one, three, six and 12 months. The following parameters will be evaluated: Pain (spontaneous pain and pain with percussion) Degree of mobility Resolution of signs of infection (fistula) at the mucobuccal fold.

Radiographical evaluation will be performed to each patient immediately after the final restoration and three, six and 12 months postoperatively.

The decrease of radiolucency and the presence of internal or external root resorption will be evaluated.

Bacteriology :

The microbiological evaluation will be done at the Biotechnology Research Institute - Suez Canal University.

PCR will be used for detection of Enterococcus faecalis. Microbiological investigation will be used for counting the number of Enterococcus faecalis.

详细描述

45 teeth will be sub-divided at random with a computerized method, according to the type irrigant and duration of its application into 3 groups (15 teeth in each group):

Group1(control group):

The teeth will be irrigated by 2 ml 1% NaOCl after each file.

Group2:

The teeth will be irrigated by 2 ml 1% NaOCl after each file then with 5 ml of 0.2% chitosan for one minute.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
3 Months 至 7 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Apparently healthy Children aged from three to seven years.
  • No previous history of antibiotics for at least two weeks.
  • Non- Vital primary teeth that can be fully isolated.
  • Presence of clinical signs or symptoms suggesting a non-vital tooth, such as intra-oral fistula.
  • Infection diagnosed by presence of periapical radiolucency in a periapical radiograph.
  • Root resorption not more than one third of the root.
  • Patient and parent cooperation.

排除标准

  • Non-restorable tooth
  • Serious reduction in bone support and/or extreme tooth mobility.
  • Radiographic indication of extensive internal or external root resorption.

结局指标

主要结局

Spontanous Pain

时间窗: after one month, 3 months, six months and 12 months

Visual analog scale "A scale from 1 to 10 where 1 is mild pain and 10 Worst pain"

Radiographic examination " internal or external root resorption"

时间窗: immediately after restoration, 3 months, six months and 12 months

Presence (1) or absence (0)

Radiographical evaluation

时间窗: immediately after restoration, 3 months, six months and 12 months

The change of radiolucency

Bacteriology

时间窗: During procedure

PCR will be used for detection of Enterococcus faecalis. \- Microbiological investigation will be used for counting the number of Enterococcus faecalis

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验