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Inhaled PGE1 in neonates with hypoxemic respiratory failure: two pilot feasibility randomized clinical trials
Journal article   Open access   Peer reviewed

Inhaled PGE1 in neonates with hypoxemic respiratory failure: two pilot feasibility randomized clinical trials

Beena G Sood, Martin Keszler, Meena Garg, Jonathan M Klein, Robin Ohls, Namasivayam Ambalavanan, C Michael Cotten, Monica Malian, Pablo J Sanchez, Satyan Lakshminrusimha, …
Trials, Vol.15(1), pp.486-486
12/12/2014
DOI: 10.1186/1745-6215-15-486
PMCID: PMC4414424
PMID: 25496504
url
https://doi.org/10.1186/1745-6215-15-486View
Published (Version of record) Open Access

Abstract

Inhaled nitric oxide (INO), a selective pulmonary vasodilator, has revolutionized the treatment of neonatal hypoxemic respiratory failure (NHRF). However, there is lack of sustained improvement in 30 to 46% of infants. Aerosolized prostaglandins I2 (PGI2) and E1 (PGE1) have been reported to be effective selective pulmonary vasodilators. The objective of this study was to evaluate the feasibility of a randomized controlled trial (RCT) of inhaled PGE1 (IPGE1) in NHRF. Two pilot multicenter phase II RCTs are included in this report. In the first pilot, late preterm and term neonates with NHRF, who had an oxygenation index (OI) of ≥15 and <25 on two arterial blood gases and had not previously received INO, were randomly assigned to receive two doses of IPGE1 (300 and 150 ng/kg/min) or placebo. The primary outcome was the enrollment of 50 infants in six to nine months at 10 sites. The first pilot was halted after four months for failure to enroll a single infant. The most common cause for non-enrollment was prior initiation of INO. In a re-designed second pilot, co-administration of IPGE1 and INO was permitted. Infants with suboptimal response to INO received either aerosolized saline or IPGE1 at a low (150 ng/kg/min) or high dose (300 ng/kg/min) for a maximum duration of 72 hours. The primary outcome was the recruitment of an adequate number of patients (n = 50) in a nine-month-period, with fewer than 20% protocol violations. No infants were enrolled in the first pilot. Seven patients were enrolled in the second pilot; three in the control, two in the low-dose IPGE1, and two in the high-dose IPGE1 groups. The study was halted for recruitment futility after approximately six months as enrollment targets were not met. No serious adverse events, one minor protocol deviation and one pharmacy protocol violation were reported. These two pilot RCTs failed to recruit adequate eligible newborns with NHRF. Complex management RCTs of novel therapies for persistent pulmonary hypertension of the newborn (PPHN) may require novel study designs and a longer period of time from study approval to commencement of enrollment. CLINICALTRIALS.GOV: Pilot one: NCT number: 00598429 registered on 10 January 2008. Last updated: 3 February 2011. Pilot two: NCT number: 01467076 17 October 2011. Last updated: 13 February 2013.
 Respiratory Insufficiency - physiopathology Hypoxia - drug therapy United States Humans Respiratory Insufficiency - diagnosis Administration, Inhalation Treatment Outcome Hypoxia - diagnosis Alprostadil - administration & dosage Feasibility Studies Patient Selection Persistent Fetal Circulation Syndrome - diagnosis Persistent Fetal Circulation Syndrome - drug therapy Early Termination of Clinical Trials Pilot Projects Sample Size Time Factors Aerosols Hypoxia - physiopathology Vasodilator Agents - administration & dosage Infant, Newborn Persistent Fetal Circulation Syndrome - physiopathology Respiratory Insufficiency - drug therapy

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