CTRI/2025/07/090804尚未招募Unknown
Evaluation of efficacy of Ropivacaine hydrochloride with Dexamethasone in third molar surgery
RUKMINI1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2025年8月11日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- 1)duration of soft tissue anesthesia
研究概览
简要总结
This is a spilt mouth study done in patients with bilaterally impacted mandibular third molars by administrating 0.75% Ropivacine with 4mg Dexamtheasone and 2%Lidocaine with 4mg Dexamethasone to assess its efficacy for duration of soft tissue anesthesia, pain, swelling and mouth opening on postoperative days 3,5 and 7.
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- All
入选标准
- •all patients who desire surgical extraction of non infected bilaterally impacted lower third molar 2)age group above 18 years 3)both sexes should be included 4)patients with no presenting acute systemic illness such as fever, common cold 5)patients who agree to enroll in the study 6)be available for follow up examinations.
排除标准
- •a history of systemic diseases that contraindicate surgical intervention 2)compromised health conditions,which would affect wound healing 3)acute infection in the surgical site 4)documented allergy to any materials utilised in the study 5)opting out of participating in the study 6)patient with a history of psychiatric disorder 7)pregnancy or lactation.
结局指标
主要结局
1)duration of soft tissue anesthesia
时间窗: intra operatively,
2)pain
时间窗: intra operatively,
3)swelling
时间窗: intra operatively,
4)mouth opening
时间窗: intra operatively,
次要结局
- 1)SWELLING(2)MOUTH OPENING)
研究者
RUKMINI
Ragas Dental College and Hospital
研究点 (1)
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