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临床试验/NCT02879630
NCT02879630已完成不适用

Prospective Evaluation of Adjusted Body Weight Dosing of Acyclovir in Obesity

West Virginia University2 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2016年11月28日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
13
试验地点
2
主要终点
Area under the curve (AUC) of systemic acyclovir exposure in obese and non-obese patients

研究概览

简要总结

Patients receiving acyclovir as standard of care will be enrolled into this study. The currently recommended dosing strategy at our institution for obese patients is to receive intravenous acyclovir dosed per an adjusted body weight [IBW + 0.4(TBW-IBW)]. They will have blood drawn once prior to the first dose of acyclovir and 10 times thereafter, over a total time period of 12 hours. These patients will already be hospitalized for other reasons, and will not be required to make additional trips to the hospital. A total of approximately 4-5 tablespoons of blood will be drawn for this study. Ten obese patients and 10 matched control (non-obese) patients will be enrolled.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

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

入选标准

  • Age ≥18 years of age
  • Receiving intravenous acyclovir 5 mg/kg (TBW for normal weight patients and ABW40 for obese patients) as part of their routine care
  • Weight > 190% of ideal body weight (IBW) for "obese" patients or weight 80-120% of IBW for matched control patients.

排除标准

  • Receipt of acyclovir or a pro-drug of acyclovir (valacyclovir, ganciclovir, valganciclovir, famciclovir) in the prior 24 hours
  • Serum creatinine >1.5 mg/dL
  • Hypersensitivity to acyclovir
  • Patients requiring ventilator support or vasopressors in the prior 24 hours
  • Receipt of probenecid, mycophenolate, tenofovir, or zidovudine in the prior 7 days
  • Significant anatomical deformities that influence body habitus (i.e. amputation)
  • Prior inclusion in this study

研究组 & 干预措施

Obese Patients

Obese patients (patients whose weight is >190% of ideal body weight) will be receive a single dose of I.V. acyclovir sodium 5mg/kg dosed by adjusted body weight as part of their routine care.

Non-obese Patients

Normal weigh patients (patients whose weight is 80-120% of ideal body weight) will be receive a single dose of I.V. acyclovir sodium 5mg/kg dosed by total body weight as part of their routine care.

结局指标

主要结局

Area under the curve (AUC) of systemic acyclovir exposure in obese and non-obese patients

时间窗: 12 hours

次要结局

  • Time that concentration is above IC50 for varicella and herpes viruses in obese and non-obese patients(12 hours)
  • Systemic Clearance of acyclovir in obese and non-obese patients(12 hours)
  • Half-life of acyclovir in obese and non-obese patients(12 hours)
  • Maximum concentration (Cmax) of acyclovir in obese and non-obese patients(12 hours)
  • Time to maximum concentration (Tmax) of acyclovir in obese and non-obese patients(12 hours)
  • Volume of distribution (Vd) of acyclovir in obese and non-obese patients(12 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Aaron Cumpston, PharmD, BCOP

Pharmacy Clinical Specialist

West Virginia University

研究点 (2)

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