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Prospective Evaluation of Adjusted Body Weight Dosing of Acyclovir in Obesity

Obesity Clinical Trial

Official title:
Prospective Evaluation of Adjusted Body Weight Dosing of Acyclovir in Obesity

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02879630
Study type Observational
Source West Virginia University
Contact Pam Bunner
Phone 304-598-4511
Email bunnerp@wvumedicine.org
Status Recruiting
Phase
Start date August 2016
Completion date December 2024
View Details
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