About this trial
Cardiovascular (CV) disease is a major morbidity in children after kidney transplantation (KTx), limiting life expectancy and impairing graft function. Arterial hypertension (AH) is the dominant CV risk factor, and highly abundant in this patient group. AH can cause left ventricular hypertrophy (LVH), which is predictive of CV death. LVH can be non-invasively assessed by measuring left ventricular mass index (LVMI). Analyses of observational data showed that blood pressure (BP) levels \<75th percentile (pct) were associated with a significant reduction of LVMI. Guidelines give BP goals for children with chronic kidney disease (CKD). No guidelines, however, exist on the treatment of AH in pediatric KTx patients. In the proposed multicenter, randomized, parallel group trial with blinded endpoint evaluation we aim to assess n=500 pediatric patients \>12 months after KTx at several KTx centers. Patients will be randomly assigned 1:1 to an intensified BP management group (BP target ≤60th pct) and a standard BP management group (BP target \<90th pct). The primary endpoint is LVMI after 24 months. Secondary endpoints are estimated glomerular filtration rate (eGFR), pulse wave velocity (PWV) and intima media thickness (IMT) after 24 months. BP control will be guaranteed for both groups through BP telemonitoring, which will be transmitted in real time to the treating physician and the trial's centralized BP office. By defining the adequate BP goal, the results of the proposed study will have direct implications for the care of children after KTx. The results will define an important element of post-KTx care and help to lower CV morbidity and subsequently CV mortality of pediatric KTx patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Kidney transplantation >12 months ago
Arterial hypertension
Disqualifiers
Cardiac malformation
Treatment for a rejection episode within three months prior to inclusion
Trial design
Parallel
Treatments tested in this trial
Intensified BP control
Other interventionTreatment goal in the intensified group will be lowering BP ≤60th pct.
Standard Treatment
Other interventionStandard treatment is to achieve BP levels \<90th pct.
Treatment groups
Trial outcomes
Primary outcomes
Left ventricular mass index (LVMI)
LVMI at 24 months after randomization. Echocardiography will follow a standardized operating procedure established during the 4C study in accordance with the American Society of Echocardiography guidelines. LVMI will be calculated by dividing left-ventricular mass in grams (according to Devereux) by height in meters to the 2.16th with a correction factor of 0.09.
Secondary outcomes
Pulse Wave velocity (PWV)
PWV at 24 months after randomization.
Estimated Glomerular Filtration Rate (eGFR)
eGFR estimated by the Schwartz bedside formula at 24 months after randomization.
Intima Media Thickness (IMT)
IMT at 24 months after randomization. IMT will be assessed using ultrasound with a high-resolution linear probe, by averaging five measurements from the far wall of the common carotid artery 1-2 cm proximal of the carotid bulb, following the Mannheim consensus.
Other outcomes
Albuminuria
Albuminuria at 24 months after randomization. Albumine to creatinine ratio from spot urine will be assessed.
Locations
Sponsors and contacts
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Hannover Medical School
Lead sponsor
Heidelberg University
Collaborator
Berlin; Charité
Collaborator
Bonn; Kindernieren-zentrum Bonn
Collaborator
University Hospital, Essen
Collaborator
Frankfurt; Clementine Kinderhospital
Collaborator
Universitätsklinikum Hamburg-Eppendorf
Collaborator
Stuttgart; Olgahospital
Collaborator
Hacettepe University
Collaborator
Vienna; University Hospital Vienna
Collaborator
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