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临床试验/CTRI/2023/05/052189
CTRI/2023/05/052189已完成2/3 期

Efficacy of 2% lignocaine combined with dexmedetomidine in comparison with 2% lignocaine with 1:80,000 adrenaline in mandibular third molar surgery : A randomised clinical trial

Chhattisgarh Dental College and Research Institute1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年5月25日最近更新:

试验速览

阶段
2/3 期
状态
已完成
入组人数
50
试验地点
1
主要终点
Onset of Anesthesia

研究概览

简要总结

Title: EFFICACY OF 2% LIGNOCAINE WITHDEXMEDETOMIDINE IN COMPARISON TO2% LIGNOCAINE WITH 1:80,000 ADRENALINE IN MANDIBULAR THIRD MOLAR SURGERY: A RANDOMISED CLINICAL TRIAL

Aim: The aim of the study is to compare the efficacy of 2% plain lignocaine combined with dexmedetomidine and 2% lignocaine with 1:80,000 adrenaline for the removal of mandibular impacted third molars.

Objective: The objective of this study is to assess the efficacy of 2% lignocaine combined with dexmedetomidine in comparison to 2% lignocaine with adrenaline for impacted mandibular third molar surgery with regards to following parameters:

ï¬ Onset of anaesthesia

ï¬ Duration of anaesthesia

ï¬ Post-operative pain

ï¬ Oedema

ï¬ Trismus

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 30.00 Year(s)(—)
性别
All

入选标准

  • ASA I (Healthy patients)
  • Patients with Pederson’s difficulty index score 5-6 (moderately difficult)
  • Patients willing for third molar extraction and participating in the study.

排除标准

  • Impacted third molars associated with acute infections or pathologies.
  • Pregnant and lactating females and patients on oral contraceptives.
  • Medically compromised patients (hypertension, bradycardia, hypotension, sinus disorder, liver disorders, renal impairment and uncontrolled diabetes)
  • Tobacco chewers and smokers.
  • Patients allergic to lignocaine with dexmedetomidine, lignocaine, and adrenaline.

结局指标

主要结局

Onset of Anesthesia

时间窗: 24 hours, 72 hours, 120 hours, 168 hours

Duration of Anesthesia

时间窗: 24 hours, 72 hours, 120 hours, 168 hours

Pain

时间窗: 24 hours, 72 hours, 120 hours, 168 hours

Mouth Opening

时间窗: 24 hours, 72 hours, 120 hours, 168 hours

To study the efficacy of dexmedetomidine combined with 2% lignocaine on:

时间窗: 24 hours, 72 hours, 120 hours, 168 hours

Edema

时间窗: 24 hours, 72 hours, 120 hours, 168 hours

次要结局

  • To compare the efficacy of 2% lignocaine combined with dexmedetomidine to 2% lignocaine with 1:80,000 adrenaline(24 hours, 72 hours, 120 hours, 168 hours)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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