A Study to Evaluate the Clinical Epidemiology of Patients With Heart Failure (HF) in India

NCT ID: NCT02047526

Last Updated: 2014-01-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2013-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This non-interventional, prospective, multi-centric, cross-sectional study is aimed to observe clinical practice in India in managing Heart Failure patients \& to check one year outcome in HF patients. A total of 5 visits will be conducted during the study. There will be a baseline visit followed by four follow-up visits to assess the outcomes

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

A non-interventional, prospective study to evaluate the clinical epidemiology of patients with Heart Failure (HF) in India

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Heart Failure

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

1

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Provision of subject informed consent
2. Female or male aged 18 years and over
3. All patients with Dyspnea and/or signs of systemic congestion

Exclusion Criteria

1. Subjects with Current Acute Coronary Syndrome
2. Absence of cardiac disease/structural heart disease
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Ammar Raza, MBBS, DIP DIAB, MBA

Role: STUDY_DIRECTOR

AstraZeneca Pharma India Ltd.

R R Kasliwal, DM

Role: PRINCIPAL_INVESTIGATOR

Medanta, The Medicity, Gurgaon

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

HF Registry-India

Identifier Type: -

Identifier Source: secondary_id

NIS-CIN-XXX-2012/1

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Cohort of Heart Failure Patients
NCT03422991 COMPLETED NA
Heart Failure Patients Registry
NCT04709263 COMPLETED
FREnch Survey on Heart Failure
NCT01956539 COMPLETED
Cohort Study of Chronic Heart Failure
NCT05960890 RECRUITING NA
Chemoreflex Sensitivity in HFpEF
NCT06309537 NOT_YET_RECRUITING