Intraventricular Hemorrhage Clinical Trial
Official title:
The Risk of Intraventricular Hemorrhage With Flat Midline Versus Right-Tilted Flat Lateral Head Positions in Preterm Infant Less Than 30 Weeks of Gestation: a Multicenter Randomized Control Trial
Intraventricular hemorrhage (IVH) in preterm infants is one of many devastating consequences of prematurity that have both acute and long-term sequelae. Turning a preterm infant's head to one side may increase intracranial pressure and occlude major ipsilateral veins in the neck, which could increase cerebral venous pressure and decrease cerebral venous drainage. Keeping preterm infants' heads in a slightly elevated midline position (side or supine) during the first 168 hours(HOL) has been recommended as one of the 10 potentially better practices to reduce the incidence of IVH in preterm infants. To the best of our knowledge, there has been no systematically collected clinical data quantifying the relationship between IVH and head position in preterm infants. However, the midline head position may challenge the well-known right neonatal head position preference. This preference continues until 3-6 months of age, after which preterm neonates keep their heads mainly in midline. The best head position for preterm neonates is still to be determined. Therefore, the investigators are aiming to conduct a large scale multicenter randomized control trial on order to answer the following research question: Does keeping heads of preterm infants less than 30 weeks of gestation in flat midline (FM) throughout the first 168 HOL reduce the risk of IVH compared to right flat lateral (rFL)? We hypothesized that keeping heads of preterm infants less than 30 weeks of gestation in FM throughout the first 168 HOL would reduce the risk of IVH compared to rFL.
Investigators will randomly assign infants lying on flat (zero degree) beds to be cared for
either in a supine FM or a supine rFL head position throughout the first 168 HOL.
Investigators will mount a sign on the incubator indicating the assigned head position to be
maintained during the first 168 HOL. The goal is to keep the neonates' heads in their
assigned positions throughout the first 168 HOL unless a medical indication required a
change in position. The left flat lateral head position will be the back-up position
whenever the medical conditions of the study neonates preclude maintaining the assigned head
positions. The bedside nurse will check the correctness of the infants' head positions every
4 hours by using the built-in spirit (bubble) level of the open-bed incubators and an
L-shaped ruler. Investigators are going to use an elbow connector of HUDSON RCI circuit
(adult circuit) in a case SENSORMEDICS will be required for neonates in FM group.
Investigators will watch and record pressure ulcers or technical difficulties arising from
using high-frequency ventilation (HFV) in the infants in FM position. After their first 168
HOL, the study infants will be given routine nursing care provided in their NICU, including
a change in head position every 6-12 hours or as needed on a slightly elevated bed. For
obvious reasons, the medical team will be unmasked to the assigned head position. It will be
left for the physician discretion for controversial/diversity issue (s) in neonatal care but
it will be recorded.
Timing of HUS examinations
1. All study neonates will have two screening head ultrasounds (HUS) as follows:
1. Within first 12 HOL.
2. At about 168 HOL.
2. Otherwise, investigators will carry HUS according to established IVH diagnosis
guidelines:
1. As early as a clinical suspicion of IVH is raised.
2. When IVH is detected, then a follow up HUS is repeated within 5-7 days later.
Diagnosis of IVH:
Ultrasound technicians or physicians who have been trained to perform HUS will perform a
standard set of HUS views through the anterior fontanel with a high-quality modern real-time
portable ultrasound machine with appropriate transducers. They will capture at least six
coronal and five sagittal planes. Investigators will send a similar digital format copy of
these images and earlier images (if any) to the three study pediatric radiologists who will
be blinded to the head position assignments. They independently will report the absence or
presence, lateralization (right, left or bilateral), extension, and grade of IVH according
to Papile's grading criteria. They will send their reports to the principal investigator via
email. If their reports are inconsistent, then diagnosis and grading of IVH will be based on
the majority or the consensus among them if majority cannot be reached.
Analysis strategy for withdrawal, drop outs, and protocol violations as both of the
following when appropriate:
1. Intention to treat analysis.
2. Per protocol analysis: Including only neonates who will have normal first 12 hours of
life HUS, complete the study or develop IVH during the study period, and have their
heads kept in the assigned head positions throughout study period (first 168 HOL)or
until time of IVH diagnosis.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT04506619 -
Safety and Efficacy Outcomes Following Previously Administered Short-Term Treatment With SHP607 in Extremely Premature Infants
|
||
Recruiting |
NCT04189471 -
Recovery After Cerebral Hemorrhage
|
||
Recruiting |
NCT06043050 -
PRedicting OutcomeS in Preterm nEonates With thromboCyTopenia (PROSPECT)
|
||
Terminated |
NCT04178746 -
PRONTO: Artemis in the Removal of Intraventricular Hemorrhage in the Hyper-Acute Phase
|
||
Not yet recruiting |
NCT06045130 -
PUFAs in Preterm Infants
|
||
Completed |
NCT02400697 -
Placental Transfusion Project for Preterm Infants
|
N/A | |
Recruiting |
NCT05113381 -
The Purpose of This Study is to Determine Whether CerebroFlo™ EVD Catheter is Effective During the Treatment of IVH
|
N/A | |
Not yet recruiting |
NCT06429332 -
International Care Bundle Evaluation in Cerebral Hemorrhage Research
|
Phase 4 | |
Recruiting |
NCT03754439 -
Minimising the Adverse Physiological Effects of Transportation on the Premature Infant
|
||
Recruiting |
NCT05118997 -
Active Removal of IntraCerebral Hematoma Via Active Irrigation
|
N/A | |
Recruiting |
NCT01098890 -
Intraventricular Tissue Plasminogen Activator (tPA) in the Management of Aneurysmal Subarachnoid Hemorrhage
|
Phase 2 | |
Recruiting |
NCT05568264 -
Effects of a Physical Therapy Intervention on Motor Delay in Infants Admitted to a Neonatal Intensive Care Unit
|
N/A | |
Terminated |
NCT04538079 -
Non-invasive Objective Assessment of Hemodynamics in Preterm Neonates
|
||
Completed |
NCT00809055 -
MRI and Neurodevelopment in Preterm Infants Following Administration of High-Dose Caffeine
|
Phase 4 | |
Completed |
NCT00197392 -
Comparative Infection Rates for the Codman BACTISEAL TM External Ventricular Drainage (EVD) System
|
Phase 4 | |
Completed |
NCT03110887 -
Monitoring Outcome in Neonatal Thrombocytopenia
|
N/A | |
Recruiting |
NCT06256939 -
Therapy BRIDGE (Bringing Real-Time Instruction Via Developmental and Gestationally-appropriate Education/Coaching) Program: A Pilot Study
|
N/A | |
Recruiting |
NCT03253263 -
A Clinical Efficacy and Safety Study of OHB-607 in Preventing Bronchopulmonary Dysplasia in Extremely Premature Infants
|
Phase 2 | |
Not yet recruiting |
NCT02394678 -
Rheolytic Thrombectomy For Adult Intraventricular Haemorrhage
|
N/A | |
Completed |
NCT00875758 -
Optimizing Treatment of Post-hemorrhagic Ventricular Dilation in Preterm Infants
|
N/A |