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Completed No phase listed Observational

An Observational Study of Respiratory Syncytial Virus (RSV) Hospitalizations in Preterm Infants

ClinicalTrials.gov ID: NCT02273882

Public ClinicalTrials.gov record NCT02273882. 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 Jul 21, 2026, 9:48 AM EDT

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

Official title

The SENTINEL 1 Study: An Observational, Non-Interventional Study in the United States to Characterize Respiratory Syncytial Virus Hospitalizations Among Infants Born at 29 to 35 Weeks Gestational Age Not Receiving Immunoprophylaxis

Study identification

NCT ID
NCT02273882
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
AstraZeneca
Industry
Enrollment
497 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
Up to 12 Months
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
Nov 16, 2014
Primary completion
Aug 18, 2016
Completion
Aug 18, 2016
Last update posted
May 22, 2017

2014 – 2016

United States locations

U.S. sites
44
U.S. states
25
U.S. cities
43
Facility City State ZIP Site status
Research Site Little Rock Arkansas
Research Site Loma Linda California
Research Site Long Beach California
Research Site Los Angeles California
Research Site Orange California
Research Site Aurora Colorado
Research Site Hartford Connecticut
Research Site Orlando Florida
Research Site Atlanta Georgia
Research Site Chicago Illinois
Research Site Evanston Illinois
Research Site Kansas City Kansas
Research Site Louisville Kentucky
Research Site New Orleans Louisiana
Research Site Boston Massachusetts
Research Site Jackson Mississippi
Research Site Reno Nevada
Research Site Atlantic City New Jersey
Research Site Morristown New Jersey
Research Site Paterson New Jersey
Research Site Brooklyn New York
Winthrop University Hospital Mineola New York 11501
Research Site Mineola New York
Research Site New York New York
Research Site Rochester New York
Research Site Syracuse New York
Research Site The Bronx New York
Research Site Durham North Carolina
Research Site Greenville North Carolina
Research Site Raleigh North Carolina
Research Site Akron Ohio
Research Site Cincinnati Ohio
Research Site Cleveland Ohio
Research Site Dayton Ohio
Research Site Oklahoma City Oklahoma
Research Site Hershey Pennsylvania
Research Site Charleston South Carolina
Research Site Sioux Falls South Dakota
Research Site Memphis Tennessee
Research Site Nashville Tennessee
Research Site Galveston Texas
Research Site Houston Texas
Research Site Richmond Virginia
Research Site Marshfield Wisconsin

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02273882, 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 May 22, 2017 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02273882 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →