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临床试验/CTRI/2025/10/096399
CTRI/2025/10/096399尚未招募2 期

Evaluation of safety and efficacy of Curcumin- Piperine- Lycopene combination versus Calcium Hydroxide as Intracanal Medicaments on pain relief in symptomatic Irreversible Pulpitis.

Dr Krishna prasad Biswas1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年11月17日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
The curcumin-based group is expected to show a statistically significant reduction in inter-appointment pain and tenderness better or comparable outcome to traditional agents like calcium hydroxide .

研究概览

简要总结

This study is randomized double blind parallel group trial comparing the safety and efficacy of Curcumin 500 mg, Piperine 5 mg, Lycopene 10 mg combination and Calcium Hydroxide as intracanal medicament for 7 days in 60 patients with symptomatic irreversible pulpitis that will be conducted in AIIMS Guwahati. The primary outcome likely that Curcumin based combination is expected to show a statistically significant reduction in inter-appointment pain and tenderness better or comparable to calcium hydroxide measured at 1st, 3rd, 5th and 7th day.

研究设计

研究类型
Interventional
分配方式
Randomized
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

  • Patient visiting Out Patient Department at AIIMS Guwahati ii.
  • Single rooted maxillary and mandibular teeth with irreversible pulpitis iv.Informed Consent.

排除标准

  • Failure to give consent ii.
  • Medically comprised iii.
  • Pregnant patient iv.
  • More than 1 root canal in tooth v.
  • Teeth with Periapical radiolucency vi Had taken medication within 12 hrs of study.

结局指标

主要结局

The curcumin-based group is expected to show a statistically significant reduction in inter-appointment pain and tenderness better or comparable outcome to traditional agents like calcium hydroxide .

时间窗: 1st day 3rd day 5th day 7th day

The study anticipates fewer analgesic requirements

时间窗: 1st day 3rd day 5th day 7th day

With better healing and recovery, prognosis of root canal treated teeth will be improved.

时间窗: 1st day 3rd day 5th day 7th day

次要结局

未报告次要终点

研究者

发起方
Dr Krishna prasad Biswas
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Krishna Prasad Biswas

AIIMS Guwahati

研究点 (1)

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