Comparison Between Two Analgesic Methods for Pain Relief Following Surgical Abortion
试验速览
- 阶段
- 不适用
- 入组人数
- 82
- 试验地点
- 1
- 主要终点
- Pain
研究概览
简要总结
To compare between the efficacy of Paracetamol IV vs. Lornoxicam IV in pain relief following surgical abortion.
The medication will be given at the time of the procedure. Following the abortion, pain level will be evaluated.
详细描述
Patients with medical indication for surgical abortion during first trimester will be divided to two groups. The study groups, the surgeons and the nurses will be blinded to one of the treatment arms.
Pain will be evaluated at fixed intervals following the abortion. Comparison in pain levels between the study groups will be analysed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Elective surgical abortion for first trimester pregnancy
排除标准
- •Chronic pelvic pain
- •Fibromyalgia
- •Pelvic inflammatory disease
- •Chronic renal failure, liver disease, peptic ulcer
- •cervical stenosis
研究组 & 干预措施
Paracetamol
Pain treatment, aniline analgesics
干预措施: Paracetamol (Drug)
Paracetamol
Pain treatment, aniline analgesics
干预措施: lornoxicam (Drug)
lornoxicam
Pain treatment, nonsteroidal anti-inflammatory (NSAID)
干预措施: Paracetamol (Drug)
lornoxicam
Pain treatment, nonsteroidal anti-inflammatory (NSAID)
干预措施: lornoxicam (Drug)
结局指标
主要结局
Pain
时间窗: Two hours
Pain level will be evaluated by VAS
次要结局
未报告次要终点
研究者
Lior Lowenstein
Gynecologist
Rambam Health Care Campus