Clinical Trial Details
— Status: Not yet recruiting
Administrative data
NCT number |
NCT04885088 |
Other study ID # |
ShuangHoH |
Secondary ID |
|
Status |
Not yet recruiting |
Phase |
|
First received |
|
Last updated |
|
Start date |
July 1, 2021 |
Est. completion date |
June 30, 2023 |
Study information
Verified date |
May 2021 |
Source |
Taipei Medical University Shuang Ho Hospital |
Contact |
YU ANN FANG, MS |
Phone |
886-2-22490088 |
Email |
runawayyu[@]hotmail.com |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
Thoracic malignancy is the most commonly diagnosed cancer worldwide.1,2 The incidence of
thoracic malignancy has decreased in North America, but not in Asia, where it continues to
show an increasing trend. A notable manifestation of the bimodal age distribution of thoracic
malignancy has been observed in women. The occurrence of early-onset thoracic malignancy in
the Asian population is earlier than that in the Western population, resulting in a higher
incidence of thoracic malignancy in young Asian women. Moreover, the late onset age
distribution of patients with thoracic malignancy in Asia (40-50 years) is earlier than that
in Western countries (60-70 years), peaking at the age of 45-50 years in most women. The
age-specific incidence rates of thoracic malignancy increase sharply until the menopausal
stage.
Cardiovascular morbidity is higher among women with thoracic malignancy involving the thorax
who had received radiotherapy (RT) compared with those not involving the thorax but receiving
the same treatment. Thus far, the risks and time to onset of cardiac complications have been
unclear in both young and old women. The proportion of young women with thoracic malignancy
is higher in Asia than in Western countries. Furthermore, whether Asian women with thoracic
malignancy are susceptible to RT remains unclear.
Anthracyclines are important therapeutic agents for breast cancer. Anthracycline-based
regimens have similar or improved outcomes relative to the standard treatment regimen of
cyclophosphamide, methotrexate, and fluorouracil. However, cardiotoxicity is a long-term
toxicity associated with these regimens. The combined use of adjuvant anthracycline-based
chemotherapy (CT) and RT may result in high cardiotoxicity. Nonetheless, no clear information
on the effects of this combined therapy on the time to onset of both cardiac complications
and cardiotoxicity is available. Furthermore, whether the cardiotoxicity of adjuvant RT and
anthracycline-based CT is associated with age and ethnicity in women with thoracic malignancy
remains unclear.
Therefore, cardiovascular disease is undoubtedly one of the most challenging health problems
in the world. More efforts are needed to prevent and better control of this disease. Our
proposed monitoring program is to use AI to monitor the basal value variation of personalized
cardiovascular disease in cancer patients before and after chemoradiation. In the first year,
our team focused on cardiotoxicity associated with cardiovascular disease models and cancer
treatments. In the second year, we will apply knowledge in a clinical setting and calculate
the severity of cardiac toxicity and its incidence and time response after cancer treatment.
In the third year, high-risk groups will be identified to provide preventive intervention to
reduce the risk of cancer-treatment related cardiotoxicity.
Description:
This study is open, prospective study, multi-center, randomized controlled trial, unobtrusive
research. This study is start on June 1 2021. And will include 400 patients who have just
cardiotoxicity of adjuvant RT and anthracycline-based CT patients who diagnosis of Thoracic
malignancy. And random allocation 200 experimental group (Non-invasive Wearable Device) and
200 control group (routine medical).
Ask whether the patients who meet the exclusion criteria are willing to participate in the
screening (Screening), if they are willing to join and sign the consent of the subject, and
after the patient's condition is stable, conduct an electrocardiogram (V0) before discharge
from the hospital. On day 7 (±2 weeks), day 84 (±4 weeks), 168 days (±4 weeks), 252 days (±4
weeks), 336 days (±8 weeks) during routine clinical referral (V1-V5) Both are done once. The
results of these two tests and other basic information of the patient, including Demography,
Vital Signs, High, Weight, Medication, and European and Taiwan Cardiology Association
recommended routine test results of high-risk patients, including Blood Chemistry Panel,
NT-proBNP, Echocardiography, Myocardial Perfusion Scan, etc., will record the information of
the logged-in subjects on the paper case report form. The CRF only displays the study number,
and no subject is available. In addition to the examination of each return visit, the
subjects also took the ECG bracelet home at the time of discharge (V0) and wore it every day.
After the discharge, the ECG was measured every morning and evening, and their personal
activity and sleep were collected. Relevant information. After the subject was discharged
from the hospital, the subject tracked the date of all adverse events due to cardiovascular
disease within one year, including: heart failure, restenosis due to blood vessel, and
non-fatal myocardial infarction , To do blood vessel-related surgery again, and data on the
occurrence of death.