Intensified BP control
OtherTreatment goal in the intensified group will be lowering BP ≤60th pct.
NCT Number: NCT06589947
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.
Trial opening soon.
Get Notified6 year–18 year
All sexes
Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Treatment goal in the intensified group will be lowering BP ≤60th pct.
Standard treatment is to achieve BP levels <90th pct.
Time frame: At 24 months after randomization
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
PWV at 24 months after randomization.
Time frame: At 24 months after randomization
eGFR estimated by the Schwartz bedside formula at 24 months after randomization.
Time frame: At 24 months after randomization
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
Albuminuria at 24 months after randomization. Albumine to creatinine ratio from spot urine will be assessed.
Contact information is provided by the study sponsor or research team.
Anette Melk, MD PhD
CONTACT
+49 511 532 0 ext. 5597
Bernhard MW Schmidt, MD MSc
CONTACT
+49 511 532 0 ext. 2329
Hannover Medical School
Other
Acronym: SOPHOCLES
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03094702
Arterial Hypertension, Cardiovascular Diseases
Halle, Saxony-Anhalt, Germany
View Trial DetailsNCT07396792
Anemia, Arrhythmias, Cardiac
View Trial DetailsNCT07206875
Arterial Hypertension, Cardiovascular Diseases
Milan, Italy
View Trial DetailsNCT07114757
Arterial Hypertension, Brain Diseases
Latina, LT, Italy
View Trial Details