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临床试验/CTRI/2018/03/012678
CTRI/2018/03/012678尚未招募1 期

Comparing the anesthetic efficacy of 4% Articaine and 3% Mepivacaine for mandibular intraligamentary technique in patients with irreversible pulpitis- A Randomized Double - blinded clinical control trial

R Seshan Rakkesh1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年3月23日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Heft Parkers Visual Analogue Scale score below 10

研究概览

简要总结

Profound pulpal anesthesia is critical and is essential to prevent pain during endodontic treatment of diseased teeth with vital pulps. Inferior alveolar nerve block (IANB) is the most commonly used anesthetic technique for endodontic procedures in mandibular molars. Various reasons could be attributed to the failure of IANB in achieving profound pulpal anesthesia. Intraligamentary anesthetic technique has been proved to be an effective alternative to counteract this problem. Studies have shown that articaine, a long-acting amide anesthetic has better bone absorption when used as an intraligamentary injection. Similarly a short-acting local anesthetic, mepivacaine is known to produce effective pulpal anesthesia, but its efficacy, when used as an intraligamentary injection in achieving pulpal anesthesia, is not yet explored. Hence the aim of this study is to compare the efficacy of mepivacaine and articaine when used as an intraligamentary injection in achieving pulpal anesthesia of mandibular molars. Study design: 40 patients requiring root canal treatment of mandibular molars diagnosed with acute irreversible pulpitis will be selected. Patients will be randomly assigned to receive intraligamentary injections with either mepivacaine or articaine. Heft-Parker Visual Analogue Score (HP-VAS) will be used to assess pain before and after the procedure. Results: The study will be conducted and the results will be collected and statistically analysed. The primary outcome is to eliminate the pain immediately during the procedure and the secondary outcome is to observe the time taken for the anesthetic effect to wear off.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • Acute irreversible pulpitis.

排除标准

  • Systemic diseases and systemic conditions, Medically compromised, Mentally retarded patients, Local periapical pathologies, Hypersensitivity, Referred pain.

结局指标

主要结局

Heft Parkers Visual Analogue Scale score below 10

时间窗: 30 minutes

次要结局

  • Heft Parkers Visual Analogue Scale score below 10(24 hours following the procedure)

研究者

发起方
R Seshan Rakkesh
申办方类型
Other [self]

研究点 (1)

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