Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06589947

StOPping Hypertension and imprOving Children's Lives After KidnEy TranSplantation

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.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

6 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Kidney transplantation &gt;12 months ago
  • Arterial hypertension

Exclusion criteria

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

Treatment and study plan

Intensified BP control

Other

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

standard treatment

Other

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

Primary outcomes

  1. Left ventricular mass index (LVMI)

    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.

Secondary outcomes

  1. Pulse Wave velocity (PWV)

    Time frame: At 24 months after randomization

    PWV at 24 months after randomization.

  2. Estimated Glomerular Filtration Rate (eGFR)

    Time frame: At 24 months after randomization

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

  3. Intima Media Thickness (IMT)

    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.

Other outcomes

  1. Albuminuria

    Time frame: At 24 months after randomization

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

Study contacts

Contact information is provided by the study sponsor or research team.

Anette Melk, MD PhD

CONTACT

[email protected]

+49 511 532 0 ext. 5597

Bernhard MW Schmidt, MD MSc

CONTACT

[email protected]

+49 511 532 0 ext. 2329

Sponsors and collaborators

Lead sponsor

Hannover Medical School

Other

Collaborators

  • Berlin; Charité
  • Bonn; Kindernieren-zentrum Bonn
  • Frankfurt; Clementine Kinderhospital
  • Hacettepe University
  • Heidelberg University
  • Stuttgart; Olgahospital
  • University Hospital, Essen
  • Universitätsklinikum Hamburg-Eppendorf
  • Vienna; University Hospital Vienna

Registry information

Acronym: SOPHOCLES

Important dates

Study start
2024
Primary completion
2028
Study completion
2029
First posted
Sep 19, 2024
Registry last updated
Sep 19, 2024

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.