Ultrasound guided continuous adductor canal block for postoperative pain relief after total knee arthroplasty with levobupivacaine versus levobupivacaine with dexmedetomidine- A randomized Clinical study.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- PRIMARY-1.Duration of analgesia.
研究概览
简要总结
This study is a randomised single blinded parallel group comparative trial.We intend to compare the duration of post operative pain relief,side effects,total additional analgesic requirement following continuous adductor canal block in post operative patients who have undergone single knee total knee replacement.we would like to compare levobupivacaine o.25% alone versus 0.25% Levobupivacaine with Dexmedetomedine 0.5 microgram per kg body weight.this is a single centre study done in India in a private medical college with a sample size of 40 participants in each group.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients undergoing elective TKR surgeries
- •Aged between 18 years and 70 years of age
- •American Society of Anesthesiologists (ASA) class 1 to 3.
排除标准
- •Allergy to local anaesthetic
- •Intellectual impairment or psychiatric condition precluding adequate communication
- •Bleeding disorder, trauma and infection near the procedure area.
结局指标
主要结局
PRIMARY-1.Duration of analgesia.
时间窗: 24 HOURS
SECONDARY-1.24 hour opioid consumption,
时间窗: 24 HOURS
2.success of early ambulation,
时间窗: 24 HOURS
3.patient satisfaction,
时间窗: 24 HOURS
4.Any adverse effects or complications.
时间窗: 24 HOURS
次要结局
- SECONDARY-1.24 hour opioid consumption,(2.success of early ambulation,)