Kidney Transplant Recipient Clinical Trial
Official title:
Randomized Trial to Explore the Effect of Chronotherapy Versus Conventional BP Control to Correct Abnormal Circadian BP Pattern and Improve Allograft Function in Kidney Transplant Recipients
Verified date | May 2013 |
Source | Mayo Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The purpose of this study is to identify and manage factors related to blood pressure control that impact organ function and survival in kidney transplant recipients. Loss of the circadian (relating to a 24-hour rhythm) blood pressure pattern is common in kidney transplant recipients and is associated with poor allograft kidney function. It is still unclear if restoring the normal day-night blood pressure (BP) pattern will translate into better allograft outcome. Although studies in patients with and without chronic kidney disease indicate that restoration of the normal nocturnal (night) dipping in BP is possible by changing the timing of the BP medications to cover the overnight period (chronotherapy), this has not been tested in kidney transplant patients.
Status | Completed |
Enrollment | 99 |
Est. completion date | November 2012 |
Est. primary completion date | November 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Recipient of a kidney transplant. - Age=18 years. - Stable allograft function. - Ability to give informed consent. Exclusion Criteria: - Multiorgan transplant recipients. - Kidney transplant recipients with poor allograft function. - Documented history of obstructive sleep apnea. |
Allocation: Randomized, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Mayo Clinic | Jacksonville | Florida |
Lead Sponsor | Collaborator |
---|---|
Mayo Clinic |
United States,
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* Note: There are 24 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percent drop in mean SBP at night-time compared to mean SBP in day-time | 1 year | No | |
Primary | Glomerular filtration rate | 1 year | No | |
Secondary | Awake mean SBP | 1 year | No | |
Secondary | Presence of abnormal circadian BP pattern in recipients on steroid free and CIN free IS | 1 year | No | |
Secondary | Change in LVM | 1 year | No | |
Secondary | Urinary microalbumin excretion | 4 months & 1 year | No | |
Secondary | Long term renal function | 2 years | No | |
Secondary | Cardiovascular events (stroke, heart failure, myocardial infarction) | 2 years | No |
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