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

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

Treatments tested in this trial

  • Intensified BP control
  • Standard Treatment

Treatment groups

170 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

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