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StOPping Hypertension and imprOving Children's Lives After KidnEy TranSplantation

StOPping Hypertension and imprOving Children's Lives After KidnEy TranSplantation

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06589947
Acronym
SOPHOCLES
Enrollment
170
Registered
2024-09-19
Start date
2024-09-16
Completion date
2029-03-31
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arterial Hypertension, Kidney Transplant; Complications

Keywords

Left ventricular mass, Pediatric kidney transplantation

Brief summary

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.

Interventions

OTHERIntensified BP control

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

OTHERStandard Treatment

Standard treatment is to achieve BP levels <90th pct.

Sponsors

Heidelberg; University of Heidelberg
CollaboratorUNKNOWN
Berlin; Charité
CollaboratorUNKNOWN
Bonn; Kindernieren-zentrum Bonn
CollaboratorUNKNOWN
Essen; University Hospital Essen
CollaboratorUNKNOWN
Frankfurt; Clementine Kinderhospital
CollaboratorUNKNOWN
Hamburg; University Hospital Hamburg-Eppendorf
CollaboratorUNKNOWN
Stuttgart; Olgahospital
CollaboratorUNKNOWN
Hacettepe University
CollaboratorOTHER
Vienna; University Hospital Vienna
CollaboratorUNKNOWN
Hannover Medical School
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Kidney transplantation >12 months ago * Arterial hypertension

Exclusion criteria

* Cardiac malformation * Treatment for a rejection episode within three months prior to inclusion

Design outcomes

Primary

MeasureTime frameDescription
Left ventricular mass index (LVMI)At 24 months after randomizationLVMI 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

MeasureTime frameDescription
Pulse Wave velocity (PWV)At 24 months after randomizationPWV at 24 months after randomization.
Estimated Glomerular Filtration Rate (eGFR)At 24 months after randomizationeGFR estimated by the Schwartz bedside formula at 24 months after randomization.
Intima Media Thickness (IMT)At 24 months after randomizationIMT 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

MeasureTime frameDescription
AlbuminuriaAt 24 months after randomizationAlbuminuria at 24 months after randomization. Albumine to creatinine ratio from spot urine will be assessed.

Contacts

Primary ContactAnette Melk, MD PhD
sophocles@mh-hannover.de+49 511 532 0
Backup ContactBernhard MW Schmidt, MD MSc
sophocles@mh-hannover.de+49 511 532 0

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026