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Prediction of Intraventricular Hemorrhage Using Echocardiography and Near Infrared Spectroscopy

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Moderate-severe intraventricular hemorrhage (msIVH, Grades II-IV) is a significant neurological complication among extremely low gestational age neonates (ELGANs, \<=27+6 weeks) and is associated with long-term neuro-disabilities. In Canada, msIVH affects \ 25-30% of the 1300 ELGANs born annually, with little change in incidence over last decade. Typically, it occurs between days 2-7 of age, providing a finite window of opportunity. Instituting therapies at the population level, however, exposes many low-risk infants to side effects, adversely affecting risk-benefit profile and requiring large sample sizes in trials. A targeted preventative approach, though ideal, is currently challenged by our inability to reliably identify at-risk ELGANs early after birth. Near-infrared spectroscopy (NIRS) has emerged as a promising non-invasive bedside neuromonitoring tool. Pilot studies using NIRS, including ours, found lower cerebral saturations (CrSO2) and greater periods of altered cerebral autoregulation in infants who later developed msIVH. However, a systematic planned investigation is needed to establish the predictive characteristics of NIRS-derived markers, using clinically translatable methods (cumulative burden over time-period vs. single time-point values) and identify their relative performance at different time-points during transition. Further, incorporating echocardiographic (ECHO) hemodynamic markers, known to be associated with msIVH, may allow for the establishment of robust multi-model prediction models and the gain of mechanistic hemodynamic insights to inform future management. Hence, our objective is to investigate the utility of multi-modal assessment using NIRS and ECHO for early identification of ELGANs at risk of msIVH, and generate clinically applicable predictive model(s).

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Preterm infants born \<=27+6 weeks gestational age

Locations
Other Locations
Canada
Foothillls Medical Centre
NOT_YET_RECRUITING
Calgary
Royal Alexandra Hospital
NOT_YET_RECRUITING
Edmonton
London Health Sciences Centre
NOT_YET_RECRUITING
London
Mount Sinai Hospital
RECRUITING
Toronto
Contact Information
Primary
Poorva Deshpande
poorva.deshpande@sinaihealth.ca
4165864800
Backup
Laura Thomas, MSc
laura.thomas@sinaihealth.ca
4165864800
Time Frame
Start Date: 2024-04-22
Estimated Completion Date: 2027-11-01
Participants
Target number of participants: 380
Sponsors
Collaborators: Foothills Medical Centre, Royal Alexandra Hospital, London Health Sciences Centre
Leads: Mount Sinai Hospital, Canada

This content was sourced from clinicaltrials.gov