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临床试验/CTRI/2024/03/064923
CTRI/2024/03/064923尚未招募4 期

Effectiveness of oral premedication on anesthetic success of Inferior alveolar nerve block in mandibular molars with symptomatic irreversible pulpitis using Dexamethasone and combination of Dexamethasone and Ibuprofen A double blinded randomized controlled trial

Poojamol P V1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年4月25日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
Pain

研究概览

简要总结

An Inferior Alveolar Nerve Block (IANB)is the standardized injection technique for mandibular molar teeth. However, IANB does not always result in successful pulpal anesthesia, especially in patients with Symptomatic irreversible pulpitis. The fact that patients often feel pain during endodontic treatment of teeth with Symptomatic irreversible pulpitis is a challenge for the clinician. Successful anesthesia is only achieved if no or minimal pain is achieved during access cavity preparation and canal shaping. Pain during access opening and instrumentation caused by anesthetic failure was even recorded in patients who had demonstrated positive signs of anesthesia such as numbness in the lower lip and the tip of the tongue. Thus, lip numbness was shown not to be always related to successful pulpal anesthesia. The Successful management of pain during root canal treatment is important for both patients and dentist.

Various Studies have shown that the success rate of anesthesia for pain -free endodontic access and instrumentation in teeth with irreversible pulpitis can be increased by using Supplemental buccal infiltration, periodontal ligament injection, Intraosseous anesthesia and Oral premedication. Studies have shown that use of oral premedication with NSAIDS and Steroids improved the success rate of IANB in Symptomatic irreversible pulpitis. The purpose of this study is to evaluate the effect of oral premedication with 4mg Dexamethasone and combination of 800mg Ibuprofen and .5mg Dexamethasone on the anesthetic success of IANB in patients with Symptomatic irreversible pulpitis.

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 45.00 Year(s)(—)
性别
All

入选标准

  • Healthy adult patients aged 18 to 45 years Presence of irreversible pulpitis with moderate to severe pain in mandibular molars, without any signs of periapical involvement.
  • Patients not taken analgesics for at least 12 hours before enrollment in the study.

排除标准

  • Patients with allergies and hypersensitivity to medications, local anesthetic solution, or its components Pregnant or nursing women Immunocompromised patients Patients with active sites of pathosis in the area of injection.

结局指标

主要结局

Pain

时间窗: Before premedication | 15 minutes after LA | During File insertion

次要结局

  • Pain(During Access opening)

研究者

发起方
Poojamol P V
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Poojamol P V

Government Dental College Kottayam

研究点 (1)

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