StOPping Hypertension and imprOving Children's Lives After KidnEy TranSplantation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-18
SponsorHannover Medical School

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 volunteers

Qualifiers

Kidney transplantation &gt;12 months ago

Arterial hypertension

Disqualifiers

Cardiac malformation

Treatment for a rejection episode within three months prior to inclusion

Trial design

Design model

Parallel

Treatments tested in this trial

  • Intensified BP control

    Other intervention

    Treatment goal in the intensified group will be lowering BP ≤60th pct.

  • Standard Treatment

    Other intervention

    Standard treatment is to achieve BP levels \&lt;90th pct.

Treatment groups

170 Participants
are divided into 2 treatment groups
Group A: Standard BP groupActive comparator 1 intervention
Group B: Intensified BP groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
At 24 months after randomization

Secondary outcomes

1

Pulse Wave velocity (PWV)

PWV at 24 months after randomization.

Time frame
At 24 months after randomization
2

Estimated Glomerular Filtration Rate (eGFR)

eGFR estimated by the Schwartz bedside formula at 24 months after randomization.

Time frame
At 24 months after randomization
3

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.

Time frame
At 24 months after randomization

Other outcomes

1

Albuminuria

Albuminuria at 24 months after randomization. Albumine to creatinine ratio from spot urine will be assessed.

Time frame
At 24 months after randomization

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

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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