Postoperative Analgesic Efficacy of Combined Fascial Plane Blocks After Gynecologic Oncologic Surgery
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 94
- 试验地点
- 1
- 主要终点
- Total Morphine Consumption
研究概览
简要总结
The goal of this prospective observational study is to compare the effectiveness of different postoperative analgesic techniques in patients undergoing major abdominal surgery for gynecologic oncology.
The main question is whether the combination of TAP block with Quadratus Lumborum Block (QLB) or Rectus Sheath Block (RSB) provides superior pain relief compared to TAP block alone.
All blocks were performed as part of routine clinical anesthesia practice according to the attending anesthesiologist's judgment. No randomization, allocation, or study-directed intervention was performed.
Patients were classified into three groups based on the block type they received during standard care:
Group 1: TAP Block Only
Group 2: TAP + QLB Combination
Group 3: TAP + RSB Combination
Postoperative data, including pain scores (VAS), opioid consumption, sedation level, heart rate, blood pressure, nausea/vomiting, and length of hospital stay, were collected prospectively.
The study aims to determine which block combination provides the best postoperative pain control and recovery profile in patients undergoing gynecologic oncology surgery.
详细描述
This study is a prospective observational research designed to evaluate the postoperative analgesic effectiveness of different combinations of fascial plane blocks in patients undergoing gynecologic oncology surgery.
All blocks (Transversus Abdominis Plane [TAP] block, Quadratus Lumborum Block [QLB], and Rectus Sheath Block [RSB]) were performed as part of routine clinical anesthesia practice according to the attending anesthesiologist's preference.
No intervention, randomization, or protocol-directed procedure was applied for research purposes. After data collection, patients were classified into three groups based on the block type they had received in standard care:
TAP block only
TAP + QLB combination
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Total Morphine Consumption
时间窗: Within 24 hours after surgery
Total amount of morphine (mg) administered to the patient within the first 24 hours after surgery for postoperative analgesia. Morphine use will be recorded from patient-controlled analgesia (PCA) device data or medical records.
次要结局
- Incidence of postoperative nausea and vomiting(Time Frame: 0-24 hours postoperatively)
- Postoperative pain intensity (VAS score)(0-24 hours postoperatively; VAS score (0-10))
- Time to first gas or stool passage(From the end of surgery up to postoperative 72 hours)
- Time to oral intake(From the end of surgery up to postoperative 72 hours)
- Time to mobilization(From the end of surgery up to postoperative 72 hours)
- Length of hospital stay(From surgery to hospital discharge (up to 10 days) Unit of Measure:Days)
- Intensive care unit (ICU) length of stay(From surgery to hospital discharge (up to 3 days) Unit of Measure: Days)
研究者
Ayşe Menekşe Çakır
Doctor of Anesthesiology
Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital