The Neonatal Hemorrhagic Risk Assessment in Thrombocytopenia
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Karolinska Institutet
- Study ID
- NCT04598750
- Status
- Recruiting
Conditions
- Bleeding
- Neonatal Thrombocytopenia
Eligibility Criteria
- Sex
- ALL
- Age
- 1 Day - N/A
- Healthy Volunteers
- Not accepted
Study Details
This is a prospective observational study designed to evaluate Immature Platelet Fraction or Immature Platelet Count and Platelet Function Analyzer-100/200 Closure Time-ADP (in vitro bleeding time) as markers of bleeding risk in thrombocytopenic preterm neonates admitted to the Neonatal Intensive Care Unit.
Key Dates
- Start date
- Jun 15, 2021
- Status verified
- Oct 2024
- Primary completion
- Dec 31, 2025
- Completion
- Dec 31, 2025
Study Design
- Enrollment
- 250 participants (estimated)
Primary Outcome Measure
NeoBAT score [ Time Frame: 24 hours ]
Central Contacts
- Emöke Deschmann, MD, PhD+46 73 539 5575
- Martha Sola-Visner, MD617-919-4845
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Beth Israel Deaconess Medical Center | Boston | Massachusetts | 02215 | Martha Sola-Visner, MD |
| Boston Children's Hospital | Boston | Massachusetts | 02115 | Martha Sola-Visner, MD |
| Intermountain Medical Center | Murray | Utah | 84107 | Robert Christensen, MD |
| Utah Valley Hospital | Provo | Utah | 84604 | Robert Christensen, MD |
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