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Childhood Cancer clinical trials

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NCT ID: NCT04101123 Recruiting - Cancer Clinical Trials

Children and Adolescents With Leukemia, Brain Tumors, and Sarcomas

SUPATEEN
Start date: January 1, 2020
Phase:
Study type: Observational

Aim of this study is to investigate the influence of social factors on participation and activity among children and adolescents aged 10-18 years with leukemia, brain tumors, and sarcomas. Furthermore personal and treatment-related factors and their impact on participation will be explored

NCT ID: NCT03852758 Recruiting - Childhood Cancer Clinical Trials

Green Exercise for Cancer - Creating Opportunities for Survivors

GECCOS
Start date: May 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to assess feasibility and acceptability for a trial to evaluate exercise behaviors, fatigue and exercise motivation in adolescent and young adult survivors of childhood cancer who participate in an outdoor exercise intervention compared to survivors who participate in an indoor exercise intervention. A pilot randomized cross over design will allow participants to be compared to traditional controls as well as self-controls.

NCT ID: NCT03790943 Recruiting - Clinical trials for Cardiovascular Diseases

Cardiac Dysfunction in Childhood Cancer Survivors

Cardio-Onco
Start date: February 13, 2018
Phase:
Study type: Observational

This multicenter, prospective cohort study evaluates early cardiac dysfunction in adult survivors of childhood cancer. The hypothesis of this study is that cardiac dysfunction can be detected earlier when using speckle tracking echocardiography as novel echocardiographic technique compared to conventional echocardiography.

NCT ID: NCT03604627 Recruiting - Childhood Cancer Clinical Trials

Study of Coronary Calcium Score as a Marker of Post-radiation Vascular Dysplasia in Adults Treated During Childhood for Cancer With Mediastinal Irradiation

COROCAN
Start date: June 14, 2018
Phase: N/A
Study type: Interventional

To measure coronary calcium score in adults treated during childhood or adolescence for irradiation cancer in the heart and / or anthracycline area and compare them to determine whether irradiation of the heart area is associated with increased calcium score after adjustment for other cardiovascular risk factors (age, sex, smoking, dyslipidemia, obesity, diabetes, high blood pressure and renal failure).

NCT ID: NCT03543852 Recruiting - Childhood Cancer Clinical Trials

SurvivorLink: Scalability of an Electronic Personal Health Record

Start date: June 14, 2021
Phase: N/A
Study type: Interventional

Previous research suggests that children and adolescents with cancer are at heightened risk of late effects that can occur months or years after cancer treatment, yet little is known about programs that increase their return for follow-up cancer care and late effects surveillance. This study will evaluate the impact of an electronic personal health record and education system, SurvivorLink, for pediatric cancer survivors and their caregivers. The researchers will develop a standardized intervention and training for the SurvivorLink trial, followed by conducting a Hybrid Type 1 effectiveness-implementation, clustered randomized, waitlist control trial to evaluate the impact of SurvivorLink on pediatric cancer patients' one year follow-up visits and completion of screening tests. The study will also assess the impact of SurvivorLink on caregiver's patient activation, survivor's and caregiver's quality of life, and self-efficacy to manage a chronic condition. This study will provide the evidence base about the effects of the system to improve follow-up care for children and adolescents with cancer and best practices for implementation for pediatric cancer centers.

NCT ID: NCT03297034 Recruiting - Childhood Cancer Clinical Trials

Swiss Childhood Cancer Survivor Study

SCCSS
Start date: January 1, 2007
Phase:
Study type: Observational [Patient Registry]

The SCCSS is designed to investigate which long-term effects childhood cancer and its treatment have on survivors, and includes those who were under 20 years when they were diagnosed. The SCCSS explores childhood cancer survivors' quality of life, the health care received by childhood cancer survivors during follow-up care, the effects of medication, somatic and psychosocial health issues, how childhood cancer survivors take care of their own health, and also collects demographic details like family background, education and profession. To learn more about these topics, the investigators send questionnaires to childhood or adolescent cancer survivors. The investigators use the results to inform physicians and patients, and to improve treatment of childhood cancer and follow-up.

NCT ID: NCT03286634 Recruiting - Clinical trials for Acute Lymphoblastic Leukemia

ASIA Down Syndrome Acute Lymphoblastic Leukemia 2016

Start date: April 18, 2017
Phase: Phase 2
Study type: Interventional

To evaluate the outcome of a prednisolone and low dose methotrexate based protocol in Down syndrome children with ALL (DS-ALL) in an Asia-wide study. The treatment protocol was modified based upon backbone of Taiwan Pediatric Oncology Group (TPOG)-ALL protocol in which risk classification will be guided by level of flow minimal residual disease (MRD) instead.

NCT ID: NCT03180918 Recruiting - Childhood Cancer Clinical Trials

Male Fertility Preservation Using Cryopreservation of Testicular Tissue Before Highly Gonadotoxic Cancer Treatment

Start date: January 2015
Phase: N/A
Study type: Interventional

Background: Due to the remarkable improvement in treatments these last decades, long term survival can be expected in more than 80% of childhood cancer patients. Unfortunately, cancer treatments can be harmful to the gonads and can affect reproductive and endocrine functions. While loss of fertility is a major concern for most patients, sperm cryopreservation should be offered to all pubertal male patients. For prepubertal boys, only the experimental option of testicular biopsy in order to cryopreserve testicular stem cells can be proposed. Primary aims - To cryopreserve testicular tissue of prepubertal patient receiving highly gonadotoxic oncological treatment. Secondary aims - To cryopreserve testicular tissue after failure of sperm cryopreservation in pubertal patient with high risk of infertility - To create a database in order to record clinical and biological follow-up data - To create a research biobank for future research projects Multicentric study: HUG, CHUV, UKBB

NCT ID: NCT03180827 Recruiting - Childhood Cancer Clinical Trials

Female Fertility Preservation Using Ovarian Tissue Cryopreservation Before Highly Gonadotoxic Cancer Treatment

Start date: June 2015
Phase: N/A
Study type: Interventional

Background: Due to the remarkable improvement in treatments these last decades, long term survival can be expected in more than 80% of childhood cancer patients. Unfortunately, cancer treatments can be harmful to the gonads and can affect reproductive and endocrine functions. While loss of fertility is a major concern for most patients, only the experimental option of ovarian tissue cryopreservation can be proposed to prepubertal girls with a high risk of infertility. For pubertal patient, cryopreservation of mature oocytes after ovarian stimulation can be offered if oncological treatment debut can be delayed. As it is often not possible, ovarian tissue cryopreservation can also be offered. Primary aims - To cryopreserve ovarian tissue of pre or peripubertal patient who will be receiving highly gonadotoxic oncological treatment. Secondary aims - To create a database in order to record clinical and biological follow-up data - To pool resources with Fertisave Registry - To create a research biobank for future research projects Multicentric study: HUG, CHUV

NCT ID: NCT02967341 Recruiting - Neutropenia Clinical Trials

Blood Draw Validation for Ciprofloxacin Pharmacokinetic Research in Pediatric Cancer Patients

Start date: March 2016
Phase: Phase 4
Study type: Interventional

To validate blood draws via a central venous catheter (Port A Cath ®) for pharmacokinetic studies of ciprofloxacin in patients under treatment for childhood cancer.