Postoperative Analgesic Efficacy of Intraoperative Surgeon-Guided Serratus Block: A Prospective Randomized Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- 24 hours postoperatively opioid consumption
研究概览
简要总结
Surgeon guided serratus block, which can be performed by the surgeon in participants undergoing breast reduction surgery, may reduce the sensation of pain from the surgical field in the postoperative period. Thus, participants experience less pain in the postoperative period, consume less analgesics, and there is a decrease in related complications. The aim of this study was to evaluate the effects of the intraoperative surgeon guided serratus block applied on the analgesic consumption of the participants in the first 24 hours after surgery in participants undergoing breast reduction surgery.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Patient's willingness to be included in the study
- •18-65 years
- •Operated with inferior pedicled breast reduction technique
- •The distance from the sternal notch to the nipple complex is between 25-40cm
- •Breast Usg result BIRADS 1-2
- •Patients who have not previously received RT to the breast and have no history of malignancy
排除标准
- •Patient's request/refusal not to be included in the study
- •Previous history of malignancy
- •RT story,
- •ASA 3-4-5-patient group
- •Severe organ failure
- •Alcohol, drug addiction
- •Bupivacaine allergy
- •Diagnosis of psychiatric illness and psychiatric drug use
- •Surgery lasting longer than 3 hours
- •Bleeding diathesis
研究组 & 干预措施
Group Control
No intervention will be made in this group.
Group SSPB
Surgeon guided serratus block will be applied before closing dermoglandular flaps
干预措施: surgeon guided serratus block (Other)
结局指标
主要结局
24 hours postoperatively opioid consumption
时间窗: 24 hours
In the postoperative period, patients will be given opioids according to their pain density with a patient-controlled device, and the daily Morphine consumption in Patient Controlled Analgesia device will be collected and compared between groups.
次要结局
- post-operative acute pain status, post-operative nausea-vomiting status, post-operative NRS determination of pain at rest and in motion determination of complications such as nausea, vomiting, itching, determination of the first PCA analgesic request.(24 hours)
研究者
alperen can kokten
doctor faculty member
Samsun University