CARTIER: Cardiotoxicity in the Elderly

Sponsor
AORTICA Group (Other)
Overall Status
Unknown status
CT.gov ID
NCT03981588
Collaborator
Instituto de Investigación Biomédica de Salamanca (Other)
110
2
84
55
0.7

Study Details

Study Description

Brief Summary

CARTIER (Cardiotoxicity in the elderly) is a prospective cohort study of newly diagnosed elderly cancer patients equal or greater than 65 years of age conduced in one tertiary center (Hospital Universitario de Salamanca at Spain. The study is academically funded in its integrity by The Instituto de Salud Carlos III (Spanish Ministry of Science, Innovation and Universities). The investigators of the study are the only responsible for the study design, data collection, and data interpretation. All study participants provide written informed consent. All enrolled patients will undergo serial surveys, 6-minutes walking test (6MWT), electrocardiogram, echocardiogram, blood samples, CMR, physical examinations and multidisciplinary clinical evaluations; before each chemotherapy cycle and at 3, 6, 9 and 12 months, 3 years and 5 years after finalization of chemotherapy, except for MRI that will be performed before 1st, 3rd, 5th cycles and at 3, 6, 9,12 months, 3 years and 5 years after chemotherapy ending

Condition or Disease Intervention/Treatment Phase
  • Other: Imaging studies

Detailed Description

Surveys completion and examinations will be obtained at the same day: within 72 hours before each cycle of treatment or at 3, 6, 9, 12 months, 3 years and 5 years' follow-up after ending the whole antitumoral course of treatment. A fully dedicated research nurse will play a vital role in ensuring that the study run smoothly and that all participants will be safe and fully informed. Questionnaires completion and quality of life assessment will initially be performed followed by the 6MWT. Participants blood pressure measurement, electrocardiogram and echocardiogram will be then taken >30 minutes after finishing the walking test. Blood sample extraction will be performed after echocardiography to finalize with cardiac magnetic resonance. A complete medical history, physical examination and evaluation of these examinations for each participant will be performed by a cardiologist at the cardio-oncology unit, where prevention and treatment protocols for cardiotoxicity will be applied and discussed in a multidisciplinary way with referral oncologists and hematologists before every cycle of treatment and after course of antitumoral ending follow-up.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
110 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
CARDIOTOXICITY IN THE ELDERLY
Actual Study Start Date :
Mar 1, 2015
Actual Primary Completion Date :
Dec 1, 2016
Anticipated Study Completion Date :
Mar 1, 2022

Outcome Measures

Primary Outcome Measures

  1. Incidence of cardiotoxicity [5 years]

    53% as the lower limit of ejection fraction regardless of gender

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • newly diagnosed cancer initiating antisudoral treatment

  • capability to sign the informed consent

  • capability to realize 6 minutes walking test

Exclusion Criteria:
  • previous chemotherapy

  • contraindications to undergo cardiac magnetic resonance (CMR)

  • enrollment in onco-hematologist current clinical-trials

  • clinical situation making difficult the realization of the proposed examinations or the course of chemotherapy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Universitario de Salamanca Salamanca Spain 37002
2 Pedro Dorado Salamanca Spain 37007

Sponsors and Collaborators

  • AORTICA Group
  • Instituto de Investigación Biomédica de Salamanca

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pedro L Sanchez, Head of the Cardiology Department, AORTICA Group
ClinicalTrials.gov Identifier:
NCT03981588
Other Study ID Numbers:
  • PIE14/00066
First Posted:
Jun 11, 2019
Last Update Posted:
May 27, 2020
Last Verified:
Jun 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 27, 2020