To Evaluate And Compare The Efficacy Of Inferior Alveolar Nerve Block In Symptomatic Irreversible Pulpitis Cases Using Lignocaine With Articaine And Cryotherapy As An Adjunct, In Pain Reduction During Endodontic Procedures - A Clinical Trial
试验速览
- 阶段
- 2/3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- To evaluate and compare the efficacy of IANB with 2% lignocaine hydrochloride , lignocaine with
研究概览
简要总结
The study will be done to evaluate and compare the efficacy of inferior alveolar nerve block in symptomatic irreversible pulpitis cases using lignocaine with articaine and cryotherapy as an adjunct, in pain reduction during endodontic procedures. The forthcoming clinical study will be carried out within the Department of Conservative Dentistry and Endodontics at I.T.S. Dental College, Hospital, and Research Centre in Greater Noida, Uttar Pradesh. The sample size for the study will encompass a total of 150 patients drawn from the Outpatient Department (O.P.D) of the Department of Conservative Dentistry and Endodontics, adhering meticulously to predefined inclusion and exclusion criteria. Patients will be screened according to the degree of baseline pain which will be determined before the selection of the sample using numerical rating scale (NRS). If a patient met all the inclusion criteria, he/she will be informed of the nature of the study and will be invited to participate by signing the consent forms. Patients will be then allocated to 3 groups of 50 patients each receiving standard inferior alveolar nerve block with lignocaine, standard inferior alveolar nerve block with lignocaine hydrochloride and supplementary buccal infiltration with articaine, Standard inferior alveolar nerve block with lignocaine hydrochloride followed by application of endo ice and ice sticks during access opening. The patient will be asked to quantify the pain at 3 intervals i.e pre operative, during access opening and immediately after pulp extirpation. NRS scale will be used to evaluate the intensity of pain experienced by the patients on a scale of 0-10.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- None
入排标准
- 年龄范围
- 20.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients diagnosed with symptomatic irreversible pulpitis (SIP) planned for endodontic treatment in mandibular molars.
- •Patients within the age group of 20–50 years.
- •Teeth responding to cold and EPT test with lingering pain sensation for more than 30 sec.
- •Preoperative NRS score greater than 4 (Moderate to severe pain).
- •Patient consenting to be a part of this study.
排除标准
- •Patients not willing to participate in the study.
- •Age less than 20 years and more than 50 years.
- •Patients allergic to lignocaine or articaine.
- •Immature young permanent teeth.
- •Teeth that do not respond to vitality tests (Cold test and EPT).
- •Acute and chronic alveolar abscess.
- •Calcified pulp chamber and root canals.
- •Previously filled root canals.
- •Periodontally compromised teeth.
- •Medically compromised patients.
- •Patients with a history of intake of analgesics, steroids or antibiotics in the recent past 48 h.
结局指标
主要结局
To evaluate and compare the efficacy of IANB with 2% lignocaine hydrochloride , lignocaine with
时间窗: The patient will be asked to quantify the pain at 3 intervals i.e pre operative, during access opening and | immediately after pulp extirpation
articaine and cryotherapy as an adjunct in symptomatic irreversible pulpitis cases.
时间窗: The patient will be asked to quantify the pain at 3 intervals i.e pre operative, during access opening and | immediately after pulp extirpation
次要结局
- To compare the efficacy of IANB with 2% lignocaine hydrochloride , lignocaine with(articaine and cryotherapy as an adjunct in symptomatic irreversible pulpitis cases.)
研究者
Ridha Iqbal
I.T.S Dental College Hospital And Research Centre