Tramadol Versus Diclofenac for Reducing Pain Associated With Outpatient Hysteroscopy: A Randomized Double Blind Placebo-Controlled Trial
试验速览
- 阶段
- 3 期
- 入组人数
- 210
- 试验地点
- 1
- 主要终点
- Pain during the procedure
研究概览
简要总结
The purpose of this study is to compare the effectiveness of Tramadol and diclofenac in reducing pain during outpatient hysteroscopy. Women undergoing outpatient hysteroscopy in Cairo university will be divided into 3 groups, the first group will receive Tramadol 100 mg 1 hour before the procedure, the second group will receive diclofenac 100mg 1 hour before the procedure and the third will receive a placebo. Pain will be assessed by a visual analogue scale
详细描述
Hysteroscopic examination is currently the most informative investigation for patients with abnormal uterine bleeding and infertility. Outpatient hysteroscopy involves the use of miniaturized endoscopic equipment to directly visualise the endometrial cavity, without the need of formal theatre facilities, general or regional anaesthesia.
Outpatient hysteroscopy is increasingly being used as a cost-effective alternative to in-patient hysteroscopy under general anaesthesia. Like other outpatient gynaecological procedures, however, it has the potential to cause pain severe enough for the procedure to be abandoned.
Opioid analgesics are widely used for the control of moderate to severe pain. Tramadol hydrochloride, a synthetic opioid is an orally active, clinically effective centrally acting analgesic having a lower incidence of respiratory depression, cardiac depression, side effects on smooth muscle and abuse potential as compared to typical opioid agents.
Diclofenac is a non steroidal anti inflammatory drug which inhibits the cyclooxygenase enzyme.
The study will be conducted in the outpatient hysteroscopy clinic in Cairo university hospitals. All patients attending the outpatient hysteroscopy clinic will be invited to participate in the study. The invitation will include a clear full explanation of the study and patients will provide oral consent. Written informed consent is not needed since the procedure and intervention carries almost no risk to the patient and the patient will not receive anesthesia and will be fully conscious. Only patients consenting verbally to participate will be included in the trial.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Care Provider)
入排标准
- 年龄范围
- 20 Years 至 50 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Indication to do outpatient hysteroscopy
- •Consents to the procedure
- •Postmenstrual
排除标准
- •Known allergy to tramadol or diclofenac
- •Cardiac renal or gastric disease.
研究组 & 干预措施
Tramadol
Women will receive oral Tramadol 100 mg before the procedure
干预措施: Tramadol (Drug)
Diclofenac
Women will receive oral diclofenac 100 mg before the procedure
干预措施: Diclofenac (Drug)
Placebo
Women will receive oral placebo 1 hour before the procedure.
干预措施: Placebo (Drug)
结局指标
主要结局
Pain during the procedure
时间窗: 5 minutes after starting the procedure
Women will be asked to score their pain using a visual analogue scale
次要结局
- Pain after the procedure(30 minutes after competing the procedure)
研究者
AbdelGany Hassan
Lecturer of Gynecology and Obstetrics
Cairo University
