Healthy Normotensive Volunteers
Conditions
Keywords
Chronokinetics, chronodynamics, chronopharmacology, valsartan
Brief summary
The choice of drug administration time may affect the pharmacokinetics and/or drug response, and knowledge of any such circadian rhythm-dependent effects may help to reduce side effects or to enhance efficacy. This study designed to investigate the potential influence of the time of drug administration on the pharmacokinetics and pharmacodynamics of the valsartan in healthy subjects.
Detailed description
International guidelines recommend the use of long acting, once-daily medications that provide 24h efficacy; they improve adherence to therapy and minimize BP variability with smoother and more consistent BP control. Valsartan has been approved to be used once-daily, without any specification of treatment-time in package insert. Several trials have investigated the differential effects of morning versus evening administration of valsartan in hypertensive patients, however, the results of these studies were contradicting. Furthermore, the specific administration time dependent dose response curve have not been previously investigated. So, this study designed to investigate the potential influence of the time of drug administration on the pharmacokinetics and pharmacodynamics of the valsartan in healthy subjects.
Interventions
DRUGValsartan
single oral dose of 160 mg valsartan under fasting conditions
Sponsors
Ain Shams University
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
1. At least 18 years old and not more than 45 healthy male volunteers 2. Actual weight no more than ± 30% from ideal body weight based on sex, height, and body frame 3. Who had passed all the screening parameters including physical examination, laboratory tests. 4. Who had to be able to communicate effectively with study personnel, be literate, and able to give consent. 5. diurnal active subjects with eight hour night sleep. 6. free of any drug exposure known to interfere with the pharmacokinetics/pharmacodynamics or assay of valsartan for at least 10 days prior to the study
Exclusion criteria
1. Treatment with any known enzyme-inducing/inhibiting agents within 30 days prior to the start of the study and throughout the study. 2. Susceptibility to allergic reactions to valsartan. 3. Any prior surgery of the gastrointestinal tract that may interfere with drug absorption. 4. Gastrointestinal diseases. 5. Renal diseases. 6. Cardiovascular diseases. 7. Pancreatic disease including diabetes. 8. Hepatic diseases. 9. Hematological disease or pulmonary disease 10. Abnormal laboratory values. 11. Subjects who have donated blood or who have been involved in multiple dosing study requiring a large volume of blood (more than 500 ml) to be drawn within 6 weeks preceding the start of the study. 12. Nocturnal active subjects
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pharmacokinetic parameters | blood samples will be collected for 48 hour after drug administration | Maximum plasma concentration (Cmax), |
| pharmacodynamic parameter | Blood samples will be measured at prespecified time points for 48 hour after drug administration | systolic blood pressure (mm Hg) ,diastolic blood pressure (mm Hg) |
Countries
Egypt
Outcome results
None listed