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Vasopressin Antagonist
Conivaptan for Heart Failure
N/A
Waitlist Available
Research Sponsored by Hennepin County Medical Center, Minneapolis
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up predose, 1 hour and 4 hours post dose measured on day 1, 2, 3
Awards & highlights
Study Summary
The purpose of the study is to compare the effects of conivaptan and diuretics on renal blood flow and neurohormones.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ predose, 1 hour and 4 hours post dose measured on day 1, 2, 3
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~predose, 1 hour and 4 hours post dose measured on day 1, 2, 3
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
renal hemodynamics renal blood flow and glomerular filtration rate
Secondary outcome measures
measure plasma neurohormone levels
Trial Design
3Treatment groups
Active Control
Group I: ConivaptanActive Control1 Intervention
Conivaptan will be given via IV bolus
Group II: FurosemideActive Control1 Intervention
Furosemide will be given via IV bolus
Group III: conivaptan and furosemideActive Control1 Intervention
on day 3 subjects will receive both study drugs
Find a Location
Who is running the clinical trial?
Hennepin County Medical Center, MinneapolisLead Sponsor
21 Previous Clinical Trials
12,312 Total Patients Enrolled
Astellas Pharma IncIndustry Sponsor
690 Previous Clinical Trials
232,031 Total Patients Enrolled
1 Trials studying Heart Failure
Steven R Goldsmith, MDStudy DirectorHennepin County Medical Center, Minneapolis
Frequently Asked Questions
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