CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 60 enrolled
Drug / intervention
Fluticasone propionate 230mcg for 3 Months +2 moredrug
Likely dose
Fluticasone propionate 230mcg for 3 Monthsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02024204
NCT02024204N/ACompleted

Uncontrolled Lower Respiratory Symptoms in the World Trade Center Survivor Program

NYU Langone Health·interventional·Posted Dec 31, 2013·Updated Feb 2, 2021

In Brief

A clinical study evaluating Fluticasone propionate 230mcg for 3 Months, Current Treatment or no treatment, and 1 other intervention for Lung Diseases and Medication Compliance. Completed, enrolled 60 participants across 1 site.

Detailed Summary

The purpose of this study is to understand why patients in the World Trade Center program have continuing breathing problems. This study will improve investigators understanding of breathing problems among individuals with World Trade Center exposure by allowing them to review and monitor medication use, lung function, and examine other conditions that can contribute to problems with breathing. The findings from the study will help investigators understand why some people have persistent lower respiratory symptoms (breathing problems) after their exposure to World Trade Center dust and fumes, and may help guide better management and treatment of these symptoms.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedDec 31, 2013
Enrollment StartApr 9, 2014
Primary CompletionMay 17, 2017
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 12.5 years ago

Interventions

Fluticasone propionate 230mcg for 3 Monthsdrug

Current Treatment or no treatmentdrug

Patients who had symptoms at monitoring visit but are now controlled at V1 will be asked to continue their current treatment (or no treatment) and will continue with the study. They will not be provided with any medications.

Salmeterol 21mcg for 3 Monthsdrug