CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 835 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in 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/NCT01435187
NCT01435187N/ACompleted

Prematurity and Respiratory Outcomes Program (PROP) Core Database Protocol

University of Pennsylvania·observational·Posted Sep 16, 2011·Updated Nov 7, 2016

In Brief

An observational study for Prematurity and Respiratory Disease. Completed, enrolled 835 participants across 13 sites.

Detailed Summary

In survivors of extreme prematurity to 36 weeks Post Menstrual Age (PMA), specific biologic, physiologic and clinical data obtained during the initial hospitalization will predict respiratory morbidity as defined by respiratory health care utilization and respiratory symptoms, between discharge and 1 year corrected age. This protocol describes a collaboratively developed multicenter study of very preterm infants from birth through the time of discharge from the Neonatal Intensive Care Unit (NICU) and up to 1 year of age, corrected for the degree of prematurity.

Study Details

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

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedSep 16, 2011
Enrollment StartAug 1, 2011
Primary CompletionApr 1, 2015
Study CompletionMar 1, 2016
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 14.8 years ago