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临床试验/CTRI/2022/05/042897
CTRI/2022/05/042897尚未招募未知

Efficacy and safety of tamsulosin in prevention of post-operative urinary retention in hip fracture: a randomized double-blind placebo-controlled study

AIIMS Bhubaneswar0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募

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

入选标准

  • 1.All patients undergoing hip fracture surgery (ORIF or arthroplasty)
  • 2.>=18 years of age.
  • 3.Patients willing to participate

排除标准

  • 1.History of neurogenic bladder or urological problems requiring routine intermittent catheterization
  • 2.Patients unable to take an oral medication
  • 3.Patient who would require an indwelling catheter for other reasons, or patients who needed catheterisation during admission to the emergency for voiding difficulty
  • 4.Patients with systolic blood pressure <100 mmhg or orthostatic hypotension
  • 5.Pregnant women
  • 6.Associate trauma of spine or pelvis
  • 7.Patients taking medications for lower urinary tract symptoms or who had previously undergone prostatectomy
  • 8.Patients with severe liver or kidney disease
  • 9.Patients taking strong inhibitors of CYP3A4 (ketoconazole, itraconazole, clarithromycin, ritonavir/ritonavir, lopinavir/ritonavir, or conivaptan), use of a 5-alpha reductase inhibitor medication, the use of sildenafil, tadalafil, or vardenafil, history of an allergy or sensitivity to tamsulosin or other alpha-blockers (alfuzosin, doxazosin, prazosin,
  • Terazosin, or phenoxybenzamine),
  • 10.Uncontrolled concomitant illness including, but not limited to, ongoing or active infection
  • 11.Congestive heart failure, unstable angina pectoris, cardiac arrhythmia,
  • 12.Psychiatric illness

研究者

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