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临床试验/CTRI/2024/07/070401
CTRI/2024/07/070401尚未招募4 期

Comparative evaluation of 50mg Tramadol, 0.75 PercentRopivacaine, 2 Percent Lignocaine and 4 Percent Articaine inPatients undergoing Extraction of Maxillary PosteriorTooth: Unveiling Differences in Anesthetic Action, PainManagement, and Adverse Effects – A Double BlindedRandomized Clinical Controlled Trial - NI

Dr N Akash0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1-Patients both males and females aged 20–70 years.
  • 2-Firm tooth requiring extraction.
  • 3-Patients indicated for extraction of maxillary posterior tooth.
  • 4-ASA -I and II physical status patients.
  • 5-Patients willing to participate in the study.

排除标准

  • 1-Pregnant or lactating females.
  • 2-Patients with a history of drug allergy.
  • 3-Patients presenting with any systemic diseases.
  • 4-Patients with recent history of infection for which medications were taken.
  • 5-Mobile tooth.
  • 6-Tooth or root stumps with periapical lesions and abscesses.
  • 7-RCT – Treated tooth requiring transalveolar extraction or with secondary infection.
  • 8-Deleterious personal habits.
  • 9-Patients not willing to participate in the study.

研究者

发起方
Dr N Akash

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