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临床试验/NCT03232021
NCT03232021撤回2 期

Effect of Pregabalin Administration on Catheter- Related Bladder Discomfort in Orthopedic Surgical Operations

Saint Savvas Anticancer Hospital2 个研究点 分布在 1 个国家开始时间: 2017年8月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
撤回
发起方
试验地点
2
主要终点
Percentage of postsurgical catheter-related bladder discomfort after preoperative pregabalin administration

研究概览

简要总结

The aim of this study is to assess the effect of pregabalin administration on catheter-related bladder discomfort (CRBD). The study group includes patients that are about to be subjected to orthopedic operations.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients about to be subjected to urinary operations
  • Signed informed consent

排除标准

  • Preoperative urinary bladder/kidney dysfunction as a result of spinal cord pathology
  • History of overactive ((urinary frequency>3 times at night and >8 times in 24 hours), neurogenic bladder
  • End stage renal failure
  • Central nervous system dysfunction
  • Mental illness/ substance abuse
  • Sensitivity to pregabalin
  • Preoperative administration of pregabalin for other indications
  • Recent bladder catheterization <3 months

研究组 & 干预措施

Group I

Placebo Comparator

Administration of a placebo capsule 1 hour prior to the surgical operation

干预措施: Placebo oral capsule (Drug)

Group II

Experimental

Administration of 75mg of pregabalin 1 hour prior to the surgical operation

干预措施: Pregabalin Oral Capsule [Lyrica] 75mg (Drug)

Group III

Experimental

Administration of 150mg of pregabalin 1 hour prior to the surgical operation

干预措施: Pregabalin Oral Capsule [Lyrica] 150 mg (Drug)

结局指标

主要结局

Percentage of postsurgical catheter-related bladder discomfort after preoperative pregabalin administration

时间窗: Change from preoperative status to postoperative one at 0, 1, 2, 6, 24 hours postoperatively

Assessment of discomfort will be made by a scale of four (1=no discomfort, 2=mild discomfort reported on questioning only, 3=moderate discomfort, urge to pass urine reported by the patient without questioning, 4= severe discomfort, urge to pass urine accompanied by behavioral responses, such as flailing limbs, strong vocal responses or attempts to pull the catheter out)

次要结局

  • Postoperative pain assessed by NPRS scale (Numeric Pain Rating Scale)(Total amount of analgesics in morphine analogues administered in the first 24 hours postoperatively)
  • Adverse effects of the drug(All adverse effects observed in the first 24 hours postoperatively)
  • Assessment of postoperative sedation(In the operating theatre immediately after patient's extubation)

研究者

发起方
Saint Savvas Anticancer Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Georgia Micha

Principal Investigator, Anesthesiologist,MD, MSc, PhD

Saint Savvas Anticancer Hospital

研究点 (2)

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