Comparison of Ilioinguinal/Iliohypogastric Nerve Block, Erector Spine Nerve Block and Retrolaminar Nerve Block in Terms of Post-operative Pain in Inguinal Hernia Operations
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 3
- 试验地点
- 1
- 主要终点
- Visual Analogue Scale (VAS)
研究概览
简要总结
The purpose of this study is to compare the postoperative pain of patients who underwent Inguinal Hernia surgery and the differences between 3 different postoperative nerve block techniques on postoperative pain. It will be investigated which block has the higher effect on postoperative pain and can be used to control the patient's pain.
详细描述
This observational clinical study was conducted on the General Surgery operating table in Erzincan Mengücek Gazi Training and Research Hospital operating room between 3 April and 3 October 2023, after receiving approval from Erzincan Binali Yıldırım University Faculty of Medicine Ethics Committee dated 30.03.2023 and decision number 2023-07/8. Patients planned to be included in the study were included in the study after they were informed about the study and their consent was obtained.
Criteria for inclusion in the study:
- Having ASA 1 and 2 risk scores
- Primary unilateral Inguinal Hernia operation was performed
- Patients between the ages of 18-60
Exclusion criteria:
- Patients with ASA risk score of 3 and above
- Patients who underwent Recurrent Inguinal Hernia operation
- Patients who underwent Bilateral Inguinal Hernia operation
- Pregnant Patients
- Those with Neuromuscular Disease
- Patients with Uncontrolled Diabetes Mellitus
- Patients who do not accept the study
- Patients with Cognitive Dysfunction
- Patients with a history of Local Anesthetic Drug Toxicity
- Patients with a History of Cerebrovascular Disease
- Patients with Neurological Dysfunction
- Patients with Bleeding Diathesis
- Patients with spinal deformity
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Having ASA 1 and 2 risk scores
- •Primary unilateral Inguinal Hernia operation was performed
- •Patients between the ages of 18-60
排除标准
- •Patients with ASA risk score of 3 and above
- •Patients who underwent Recurrent Inguinal Hernia operation
- •Patients who underwent Bilateral Inguinal Hernia surgery
- •Pregnant Patients
- •Those with Neuromuscular Disease
- •Patients with Uncontrolled Diabetes Mellitus
- •Patients who do not accept the study
- •Patients with Cognitive Dysfunction
- •Patients with a history of Local Anesthetic Drug Toxicity
- •Patients with a History of Cerebrovascular Disease
- •Patients with Neurological Dysfunction
- •Patients with Bleeding Diathesis
- •Patients with spinal deformity
结局指标
主要结局
Visual Analogue Scale (VAS)
时间窗: 24 Hours
The patient's Pain Score (VAS Scale) will be evaluated at the 0th hour, 4th hour, 12th hour and 24th hour postoperatively. VAS scale; 0: no pain, 10: very severe, unbearable pain. For postoperative patient monitoring, a physician who does not know the type of block applied will evaluate the patients.
次要结局
未报告次要终点
研究者
DİDEM ONK
Professor Dr.
Erzincan University