Trial Information
Feasibility of Remote Cardiac Monitoring of Post-Operative Cancer Patients Experiencing Atrial Fibrillation
Inclusion Criteria:
- Post-Operative cancer patients experiencing atrial fibrillation and otherwise
clinically ready to be discharged.
- Must attend two outpatient visits at MSKCC's cardiology practice during the study
period, as specified by the participant's Attending.
- Must be older than 21 years of age.
Exclusion Criteria:
- Non-English speaking patients
Type of Study:
Observational
Study Design:
Observational Model: Cohort, Time Perspective: Prospective
Outcome Measure:
Assess the feasibility and acceptance of continuous remote cardiac monitoring
Outcome Description:
In post-operative patients with respect to recurrence of post-operative atrial fibrillation upon discharge.
Outcome Time Frame:
4 to 6 weeks
Safety Issue:
No
Principal Investigator
Michelle Johnson, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Memorial Sloan-Kettering Cancer Center
Authority:
United States: Institutional Review Board
Study ID:
10-213
NCT ID:
NCT01253590
Start Date:
December 2010
Completion Date:
December 2012
Related Keywords:
- Post-Operative Cancer Patients Experiencing Atrial
- Fibrillation
- atrial fibrillation
- ECG monitor
- Blood pressure device
- Remote Cardiac Monitoring
- Atrial Fibrillation
Name | Location |
Memorial Sloan-Kettering Cancer Center |
New York, New York 10021 |