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COMPLETED NA

Tele-HF: Yale Heart Failure Telemonitoring Study

NCT00303212 · View on ClinicalTrials.gov ↗

Study Summary

The primary purpose of this study is to determine the effectiveness of telemonitoring compared with usual guideline-based care in preventing hospitalization for heart failure patients.

Conditions Studied

Interventions

  • OTHER Telemonitoring

Study Locations (20)

Georgia

  • Piedmont Hospital Research Institute — Atlanta
  • Morehouse School of Medicine/Cardiology — Atlanta
  • Emory University — Atlanta

Missouri

  • Truman Medical Center/Cardiology — Kansas City
  • St. Luke's Hospital / Mid-America Heart Institute — Kansas City
  • Washington University — St Louis

California

  • UC Irvine Medical Center — Orange
  • UCLA Harbor Medical Center — Torrance

Connecticut

  • Department of Cardiology at Bridgeport Hospital — Bridgeport
  • Cardiology Associates of New Haven — New Haven

Louisiana

  • Chabert Medical Center — Houma
  • Heart Clinic of Louisiana — Marrero

Alabama

  • Cardiology Associates — Mobile

District of Columbia

  • Howard University Hospital — Washington D.C.

Florida

  • Integrated Care / Cardiovascular Consultants of South Florida — Tamarac

Trial Details

FieldValue
Enrollment Target 1,660 participants
Start Date 2006-03
Est. Completion 2010-07
Phase NA

Sponsor

Yale University

1,283 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00303212

The ClinicalTrials.gov registry entry for NCT00303212 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,660 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,283 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Congestive Heart Failure appearing as the primary indexed condition, and to 1 intervention — of which Telemonitoring is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00303212 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Georgia, Missouri, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00303212 about?

NCT00303212 is a clinical study titled "Tele-HF: Yale Heart Failure Telemonitoring Study". The primary purpose of this study is to determine the effectiveness of telemonitoring compared with usual guideline-based care in preventing hospitalization for heart failure patients.

What is the current status of trial NCT00303212?

This trial is currently completed. It is a NA study. The enrollment target is 1,660 participants. The study started on 2006-03. Estimated completion is 2010-07.

What conditions does trial NCT00303212 study?

This clinical trial studies the following conditions: Congestive Heart Failure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00303212?

The interventions under investigation include: Telemonitoring (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00303212?

This trial is sponsored by Yale University, which has 1,283 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00303212 being conducted?

This trial has 20 study locations across Alabama, California, Connecticut, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial