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ECALMIST Versus InSurE in Preterm Infant < 32 Weeks,Multicenter, Multinational RCT

ECALMIST (Early CPAP And Large Volume Minimal Invasive Surfactant Therapy) Versus InSurE (Intubate, Surfactant, Extubate) in Preterm Infants With Respiratory Distress Syndrome (RDS): Prospective Randomised Control Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01848262
Acronym
ECALMIST
Enrollment
100
Registered
2013-05-07
Start date
2013-06-30
Completion date
2015-06-30
Last updated
2014-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Distress Syndrome

Keywords

ECALMIST, InSurE, CPAP, Ventilation, Vascular Catheter

Brief summary

Minimally invasive surfactant therapy via a small vascular catheter - ECALMIST (Early CPAP And Large Volume Minimal Invasive Surfactant Therapy) versus InSurE (Intubate, Surfactant Extubate) in preterm infants with Respiratory Distress Syndrome (RDS): A prospective randomized clinical trial.

Detailed description

After meeting all the inclusion criteria, eligible infants will be randomized to receive surfactant either through the ECALMIST or the InSurE methods. The attending neonatologist or neonatal team will have full discretion to decide when to intubate and when to extubate or wean the infant off the ventilator or NCPAP. General guidelines for reintubation include persistent pH\<7.20, PaCO2 \> 65 mmHg, very frequent apnea (\>2-3/hour of apneic or bradycardic spells not responsive to corrective therapy), frequent desaturations \>3/hour not responding to increase in FiO2 or increase in FiO2 to 100%), or apneas requiring prolonged PPV. For the purpose of the study a successful outcome for the primary objective will have occurred if the infant has not been reintubated and ventilated during the initial 3 days of life.

Interventions

PROCEDUREECALMIST

Surfactant administration via 17 (5 French) gauge, 133 mm length vascular catheter. 5 ml/kg will be drawn up in a 5 or 10 ml syringe. The vascular catheter will be inserted through the vocal cords under direct vision using a standard laryngoscope with the appropriate blade for gestational age. The procedure will be done without removing the NCPAP. A bolus of surfactant of 0.25-0.5 ml will be administered, after observing the surfactant moving up and down as indication of accurate intubation of the trachea. The surfactant will be slowly injected by small pulses of 0.25-0.5 ml over 20-30 seconds, each bolus with 10 seconds apart. At the end of the procedure, the operator will flush the catheter with 0.5 ml of air before removing the catheter.

PROCEDUREInSure

Patients who will receive surfactant via this technique will have their NCPAP removed and then they will be orally intubated with a standard endotracheal tube (ETT) using standard endotracheal intubation procedures using appropriate size ETT according to the birth weight. Bovine surfactant will be administered through the ETT using the same technique described above for arm 1. Manual lung inflation using a Jackson -Rees anesthesia bag at 20/5-cm H2O pressure will be performed during the surfactant instillation after which the patient will be extubated promptly as per the discretion of the neonatal team. Immediately following extubation, nCPAP support will be recommenced. No premedication, such as sedation or atropine, will be used during either procedure.

Sponsors

University of Manitoba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
24 Weeks to 31 Weeks
Healthy volunteers
No

Inclusion criteria

All should apply: * Newborn less than 32 weeks gestation at birth * Postnatal age \< 24 hrs of life * Clinical diagnosis of RDS * Spontaneously breathing on NCPAP * Clinical decision to give surfactant.

Exclusion criteria

* Lack of parental consent. * Need for mechanical ventilation * Major congenital malformation

Design outcomes

Primary

MeasureTime frameDescription
Incidence of early ventilation hours3 daysThe number of the newborn infants needed ventilation in the 1st 3 days of life

Secondary

MeasureTime frameDescription
Apnea15 minutesPause or stop of breathing for more than 20 seconds or stop of breathing that associated with decrease oxygen saturation below 75% or decrease heart rate below 100 during ECALMIST or InSurE method of surfactant therapy
Bradycardia15 minutesDecreased heart rate below 100 beat per minutes during ECALMIST or InSurE procedure
Desaturation15 minutesDecreased level of oxygen saturation measured by pulse oximeter to below 75% for more than 20 seconds during either ECALMIST or InSurE
Incidence of Chronic lung disease1st 2 months of lifeThe incidence of Chronic lung disease (CLD) both definitions; the need for oxygen support at 28 days of postnatal life and at the 36 weeks of corrected postnatal age
Early ventilation hours3 daysThe mean of ventilation hours
Total ventilation hourshospital admition daysNumber of total hours during which the newborn are ventilated during hospital admission (form delivery till discharge home)

Other

MeasureTime frameDescription
Hospital stay1st three months of lifeThe number of days that newborn spent in the hospital after delivery

Countries

Canada

Contacts

Primary ContactYahya Ethawi, MD
yalethawi@hsc.mb.ca2049634721
Backup ContactAbrar Hussain, MD
ahussain3@hsc.mb.ca2047719301

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026