跳至主要内容
临床试验/CTRI/2025/07/090779
CTRI/2025/07/090779
招募中
3 期

Evaluation of post operative pain following the use of two different file systems with two different cross- sectional designs with and without the use of preoperative analgesics: A Randomized Clinical Trial

Sonia S1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2025年8月8日最近更新:

概览

阶段
3 期
状态
招募中
发起方
Sonia S
入组人数
48
试验地点
1
主要终点
To determine the intensity of postoperative pain using visual analog scale

概览

简要总结

This double-blind randomized clinical trial aims to evaluate postoperative pain following root canal treatment in single-rooted teeth with symptomatic irreversible pulpitis using ProTaper Gold and VDW Rotate file systems with and without preoperative analgesic Zerodol-SP. Pain levels will be assessed using a visual analog scale across multiple time intervals over 3 days. The study aims to provide insight into optimal instrumentation and preoperative medication strategies for improved patient comfort.

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 Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • single rooted teeth with symptomatic irreversible pulpits, absence of periodical changes, ASA-1 category patients, patients who have not taken anti-depressants, analgesics or sedative drugs in the past 12 hours before treatment, patient who understand visual analog scale, patient willing to provide informed consent.

排除标准

  • Multi rooted teeth or teeth with periapical changes, breastfeeding or pregnant women, patient allergic to anaesthetics or NSAIDS, use of immunosuppressants, patients who have taken analgesics, anti depressants or sedative drugs in the past 12 hours, calcified and resorbed canals, complex canal anatomy, non vital pulp, unrestorable teeth, teeth with acute and chronic apical abscess, teeth with previous endodontic treatment, patient with systemic infections.

结局指标

主要结局

To determine the intensity of postoperative pain using visual analog scale

时间窗: baseline before treatment, 6 hours, 12 hours, 18 hours, 24 hours, 48 hours and 72 hours

次要结局

  • monitor analgesic consumption -number & frequency postoperatively,(monitor patient comfort,)

研究者

发起方
Sonia S
申办方类型
Other [Individual [ self sponsored ]]
责任方
Principal Investigator
主要研究者

Sonia S

Tagore dental college and hospital

研究点 (1)

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