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Spots Global Cancer Trial Database for Effect of Body Mass on Acyclovir Pharmacokinetics

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Effect of Body Mass on Acyclovir Pharmacokinetics

Official Title: Effect of Body Mass on Acyclovir Pharmacokinetics

Study ID: NCT01714180

Interventions

Study Description

Brief Summary: Studies have shown that different percentages of body fat can alter the way drugs are distributed in the body. This study will use blood samples taken at different time points for patients taking acyclovir to determine if higher body weights affect drug exposure. The information gathered from this study will help understand if patients with higher body weights need a different dosing plan. Patients receiving acyclovir as standard of care will be enrolled into this study. They will have blood draws once before they take acyclovir and 10 times after they take the acyclovir (over a total of 12 hours). These patients will be in the hospital already and will not need to make additional trips back to have blood drawn. A total of about 4-5 tablespoons of blood will be drawn for this study. 7 obese patients and 7 matched, non-obese patients will be enrolled into this study.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

West Virginia University Hospitals Mary Babb Randolph Cancer Center, Morgantown, West Virginia, United States

Contact Details

Name: Aaron Cumpston, PharmD

Affiliation: West Virginia University

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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