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Completed No phase listed Observational

An Observational Study to Assess RSV-associated Illness in Adults With COPD and/or CHF

ClinicalTrials.gov ID: NCT01455402

Public ClinicalTrials.gov record NCT01455402. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 27, 2026, 5:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Observational Study to Assess Respiratory Syncytial Virus (RSV)-Associated Illness in Adults With Chronic Obstructive Pulmonary Disease (COPD) and/or Congestive Heart Failure (CHF)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this observational study is to determine the incidence of medically attended (inpatient or outpatient) acute respiratory illnesses or events leading to worsening cardiorespiratory status (ie, acute exacerbations of chronic obstructive pulmonary disease \[AECOPD\] or worsening CHF) associated with RSV infections in high-risk adults (ie, those with severe COPD and/or advanced CHF) across multiple consecutive RSV seasons.

Study identification

NCT ID
NCT01455402
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
MedImmune LLC
Industry
Enrollment
476 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2010
Primary completion
Apr 30, 2014
Completion
Apr 30, 2014
Last update posted
Jul 8, 2014

2010 – 2014

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Research Site Birmingham Alabama 35294 —
Research Site Fort Smith Arkansas 72901 —
Research Site Denver Colorado — —
Research Site Bay Pines Florida — —
Research Site Miami Florida — —
Research Site Marietta Georgia 30060 —
Research Site Council Bluffs Iowa 51503 —
Research Site Minneapolis Minnesota — —
Research Site Reno Nevada 89502 —
Research Site Buffalo New York 14215-1199 —
Research Site Mineola New York 11501 —
Research Site Rochester New York 14621 —
Research Site Chardon Ohio 44024 —
Research Site Beaver Pennsylvania 15009 —
Research Site Jefferson Hills Pennsylvania 15025 —
Research Site Pittsburgh Pennsylvania 15213 —
Research Site Nashville Tennessee 35294 —
Research Site Houston Texas 77030 —
Research Site Kingwood Texas 77339 —
Research Site Marshfield Wisconsin — —
Research Site Milwaukee Wisconsin 53295 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 39 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01455402, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 8, 2014 · Synced Sep 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01455402 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →