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Behavioural Intervention
SNOO for Pre-eclampsia
N/A
Waitlist Available
Led By Alisse Hauspurg, MD
Research Sponsored by Alisse Hauspurg
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 months postpartum
Awards & highlights
Study Summary
This study is evaluating whether a bassinet designed to calm infants may help reduce blood pressure in women with hypertensive disorders of pregnancy.
Eligible Conditions
- Pre-eclampsia
- Hypertension
- Sleep
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 months postpartum
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 months postpartum
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Secondary outcome measures
Body Mass Index
Body Mass Index in kg/m^2
Breslau 7-Item Screen for Post-traumatic Stress Disorder Score
+16 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: SNOO Responsive BassinetExperimental Treatment2 Interventions
Will receive and be instructed on the use of the SNOO responsive bassinet for their newborn + the current standard of care of safe sleep education in the postpartum period
Group II: Usual CareActive Control1 Intervention
Will receive the current standard of care of safe sleep education in the postpartum period
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
SNOO
2021
N/A
~110
Find a Location
Who is running the clinical trial?
Happiest Baby, Inc.Industry Sponsor
1 Previous Clinical Trials
50 Total Patients Enrolled
Alisse HauspurgLead Sponsor
2 Previous Clinical Trials
120 Total Patients Enrolled
Alisse Hauspurg, MDPrincipal InvestigatorUniversity of Pittsburgh, Magee-Womens Hospital
2 Previous Clinical Trials
688 Total Patients Enrolled
Frequently Asked Questions
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