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临床试验 NCT07360028 针对Post Operative Pain Control目前招募中。请查看临床试验雷达卡片视图和 AI 发现工具了解所有详情,或在此提出任何问题。 | ||
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卡片视图
Efficacy of Ultrasound Guided Erector Spinae Plane Block Versus Ultrasound Guided Serratus Anterior Plane Block for Postoperative Pain Control Following Video-assisted Thoracoscopic Surgeries (VATS): Randomized Control Trial 50 随机化
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临床试验NCT07360028是一项针对Post Operative Pain Control的干预性研究试验,目前试验状态为招募中。试验始于2025年12月1日,计划招募50名患者。该研究由艾因夏姆斯大学主导,预计于2027年12月30日完成。试验数据来源于ClinicalTrials.gov,最后更新时间为2026年1月22日。
简要概括
The aim of the study is to compare the analgesic efficacy of Erector spinae plane block versus Serratus anterior plane block in patients undergoing video-assisted thoracoscopic surgeries.
详细描述
The aim of the study is to compare the analgesic efficacy of Erector spinae plane block versus Serratus anterior plane block in patients undergoing video-assisted thoracoscopic surgeries.
Preoperative: - On the day before surgery, all patients will be evaluated, detailed medical and surgical history will be taken also physical and systemic examinations will be done.
The following investigations will be done includi...
显示更多官方标题
Efficacy of Ultrasound Guided Erector Spinae Plane Block Versus Ultrasound Guided Serratus Anterior Plane Block for Postoperative Pain Control Following Video-assisted Thoracoscopic Surgeries (VATS): Randomized Control Trial
疾病
Post Operative Pain Control其他研究标识符
- FMASU MD 307/2025
NCT编号
实际开始日期
2025-12-01
最近更新发布
2026-01-22
预计完成日期
2027-12-30
计划入组人数
50
研究类型
干预性研究
试验分期 (阶段)
不适用
试验状态
招募中
关键词
post operative pain control
主要目的
治疗方法
分配方式
随机
干预模型
平行
盲法
双盲
试验组/干预措施
| 参与者组/试验组 | 干预措施/治疗方法 |
|---|---|
阳性对照Erectror Spinae Plane Block Ultrasound Guided block using 20 mL of 0.25% bupivacaine. | Erector Spinae (ESP) Block with Bupivacaine (Marcaine®) Ultrasound Guided Erector Spinae Plane block using 20 mL of 0.25% bupivacaine. |
阳性对照Serratus Anterior Plane Block Ultrasound Guided block using 20 mL of 0.25% bupivacaine. | Serratus anterior plane block (SAP) Ultrasound Guided Serratus Anterior Plane Block using 20 mL of 0.25% bupivacaine. |
主要终点
| 结果指标 | 度量标准描述 | 时间框架 |
|---|---|---|
Visual analogue scale for Assessing postoperative pain control | Assessing The difference in postoperative pain control between both groups as determined by assessing the visual analogue scale | after ICU admission at 2, 4, 8, 16, 24 hours post operative. |
参与助手
资格标准
适龄参与研究
成人, 老年人
最低年龄要求
25 Years
适龄性别
全部
- Patients with American Society of Anesthesiology physical status ASA I, II and III.
- Patients aged between 25 and 70 years.
- patients undergoing video-assisted thoracoscopic surgeries (VATS), including pleurectomy, bullectomy, sympathectomy, esophagectomy, decortication, lobectomy, and pneumonectomy.
- Patients below age of 25 or above age of 70.
- Patient refusal.
- Allergy to local anesthetic drugs.
- Bleeding or coagulation disorder.
- Psychiatric disorders.
- Infection at the needle entry site.
- Renal impairment (creatinine >1.5 ).
- Hepatic impairment (Child B or C).
- Patients with known Cortisol related diseases such as Cushing's Syndrome or Addison's Disease.
研究中心联系人
联系人: EMAN ZAGHLOUL MADY, MSc, 00201013177848, [email protected]
1 位于 1 个国家/地区的研究中心
Abbassia-Egypt
Ain-Shams University Hospitals, Cairo, Abbassia-Egypt, Egypt
EMAN ZAGHLOUL MADY, MSc, 联系人, 00201013177848, [email protected]
招募中