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Clinical Trials/CTRI/2021/04/032844
CTRI/2021/04/032844
Recruiting
未知

Assessing the Quality of life in hospitalized patients with heart failure

MEDANTA0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: I504- Combined systolic (congestive) anddiastolic (congestive) heart failure
Sponsor
MEDANTA
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
MEDANTA

Eligibility Criteria

Inclusion Criteria

  • Patients meeting with following criteria to be included in the study:
  • 1\) Adult patients (but not younger than18 year old) will be included
  • 2\) Completion of written informed consent before any assessment is performed.
  • 3\) Patients who will be admitted to the hospital or emergency department with a (newly or with existing) diagnosis of heart failure with HFrEF and HFmEF

Exclusion Criteria

  • Patients meeting with following criteria to be excluded from the study:
  • 1\) Currently enrolled in another interventional study
  • 2\) The patient has recently completed a clinical trial (within past 3 months) that has been terminated and other options (e.g., trial extensions, amendments, etc.) are available to continue a similar treatment, similar tools.
  • 3\) Severe cognitive dysfunction or dementia
  • 4\) Pregnant or lactating Women.
  • 5\) Patients and/or his/her legally acceptable representative not willing to provide voluntary written informed consent for participation in the study

Outcomes

Primary Outcomes

Not specified

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