CTRI/2024/04/065243尚未招募2 期
Comparision of Analgesic Efficacy of Ketoprofen delivered through Transdermal and oral routes in Post operative Pain management following Periodontal Flap Surgery.
ade.ramesh1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年5月3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
- 10
- 试验地点
- 1
- 主要终点
- To evaluate and compare the analgesic efficacy of ketoprofen administered through oral and transdermal routes following flap surgery.
研究概览
简要总结
A total of 10 apparently healthy subjects with chronic periodontitis will be selected into the study according to the inclusion and exclusion criteria.
Following the flap surgery on one quadrant, 50 mg of oral ketoprofen, twice daily for 3 days, will be prescribed. When the same patient returned for the flap surgery on the contralateral side, a 20 mg ketoprofen transdermal patch (ketoplast) will be placed once daily for 3 days.Patients will be asked verbally to assign a score for pain intensity at , 24, 48, and 72hrs postoperatively.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Outcome Assessor Blinded
入排标准
- 年龄范围
- 25.00 Year(s) 至 55.00 Year(s)（—）
- 性别
- All
入选标准
- •apparently healthy individuals.
- •patient who are giving informed consent.
- •age group of 25-55 years 4)patient with chronic periodontis.
排除标准
- •Patients with a history of allergy to propionic acid derivatives.
- •Subjects under chronic treatment with NSAIDs within 1 month.
- •Pregnancy and lactating woman.
结局指标
主要结局
To evaluate and compare the analgesic efficacy of ketoprofen administered through oral and transdermal routes following flap surgery.
时间窗: 24, 48, and 72hrs
次要结局
- To evaluate & compare the analgesic efficacy of ketoprofen administered through oral & transdermal routes following flap surgery.(24, 48, & 72hrs)
研究者
ADE RAMESH
Department of periodontics
研究点 (1)
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