PACTR202303539794048Other1 期
A randomized double-blinded clinical trial to investigate the role of ultrasound-guided transversus abdominis plane block after a radical hysterectomy of cervical cancer
适应症
试验速览
- 阶段
- 1 期
- 状态
- Other
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •All adults aged greater than 18 years old with the following criteria will be considered.
- •Patients with the classification of ASA physical status II and III
- •Patients who can tolerate a general anesthetic
- •Patients undergoing cervical cancer surgery (radical hysterectomy) under general anesthesia,
- •Patients who can provide informed consent for the surgery
- •20 ml of 0.25 % bupivacaine will be given for cases (TAP block) at the end of the surgery
- •Patients' weights are between 40-80 kg.
- •Patients who can provide informed consent for the surgery
排除标准
- •Patients who have bleeding disorders
- •Patients who are GCS <15
- •Communication failure
- •Patients who have an allergy to local anesthetics
- •Patients who have multiple site surgery (outside of abdomen)
- •Patients who have underlying cardiovascular diseases
- •Patients with chronic pain and opioid use (using oral morphine greater than 100 mg daily).
研究者
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