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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04815447
Other study ID # RECHMPL20_0089
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2020
Est. completion date February 20, 2021

Study information

Verified date March 2021
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Medical progress have made it possible to considerably improve the survival of children with an oncological disease. Currently, the survival rate increased to above 90 % in the most developed countries . This increase of childhood cancer survivors (CCS) asks us about their future and their quality of life. Assessing health related life quality , previous studies observe that in this particular population of patients, it is related to a poor physical capacity , physical activity level and many of these patients do not meet the activity level recommended by the world health organization due to fatigability and sedentary behaviours . In addition to these habits, the CCS are more susceptible to develop cardiovascular risk (CVR) leading to cardiovascular disease in adulthood and increases them mortality . Furthermore, CCS who have been experiencing hematopoietic stem cells transplantation (HSCT) are more susceptible to develop these CVR. In parallel with the common CVR, lower cardiopulmonary fitness assessed by cardiopulmonary exercise test (CPET) in the general population has been established as a major and independent CVR for cardiologic events. Cardiopulmonary fitness assessed by maximal cardiopulmonary exercise test (CPET) allows physicians to measure metabolic response to maximal effort in a population that is known as VO2max. This domain of applied physiology permits a new way to approach the understanding of global health prognosis in chronic disease. For example, decrease of VO2max is involved in lower quality of life in patients with congenital heart disease. Cardiopulmonary exercise test for VO2max exploration has been demonstrated feasible in child patients with leukemia or other tumors after intensive chemotherapy, prior to HSCT. Assessment of cardiopulmonary fitness in CCS is already described in previous studies, but this study aimed to compare a maximal CPET assessment on a large childhood cancer survivors cohort with healthy control, on a quite young cohort, during the oncologic follow up and find out its determinants.


Description:

This is a controlled, monocentric, cross-sectional study conducted in a tertiary care center for oncologic disease in children (Montpellier University Hospital, France) was carried out between November 2010 and November 2020. Two groups were identified: CCS group and control group.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date February 20, 2021
Est. primary completion date February 1, 2021
Accepts healthy volunteers No
Gender All
Age group 6 Years to 25 Years
Eligibility Inclusion criteria for CCS group : - aged between 5 and 25 years old, - having been complete a full regimen for oncological disease and considered in remission at the end of treatment. Remission was considered in absence of relapse or new treatment initiated before the CPET end point. Inclusion criteria for control group : - children referred for a nonsevere functional symptom linked to exercise (murmur, palpitation or dyspnoea) or for a medical sports certificate. - completely normal check-up, including physical examination, ECG, echocardiography and spirometry. Exclusion criteria for control group: - Children with any chronic disease, medical condition (cardiac, neurological, respiratory, muscular or renal) - Children with any medical treatment - Children requiring any further specialised medical consultation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uh Montpellier Montpellier

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Montpellier Pediatric and Congenital Cardiology Department, Montpellier University Hospital, France, Pediatric Oncology Department, Montpellier University Hospital, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary comparison of VO2max for CCS patients compared to control children comparison of the mean of VO2max value in ml/kg/min between CCS group and control group 1 day
Secondary comparison of ventilatory anaerobic threshold (VAT) for CCS patients compared to control children comparison of the mean of VAT value in ml/kg/min between CCS group and control group 1 day
Secondary correlation between clinical determinants and VO2max in the CCS group with multivariate analysis, we will look for the correlation between the clinical determinants and the decreased of VO2max in CCS group. 1 day
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