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Recruiting NCT06361303

The Happiest Baby, Inc. SNOO Postmarket Surveillance Study

— Observational Infant Death Serious Injury

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: SNOO Bassinet.
Who it may be relevant to
Registry conditions: Infant Death, Serious Injury. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

This postmarket surveillance study will evaluate the safety of the SNOO Smart Sleeper Bassinet when used for infants who are at high risk for Sudden Unexpected Infant Death (SUID). This study will survey 1000 caregivers of high-risk infants to examine the frequency of death or serious injury occurring in the SNOO Bassinet.

Detailed description

Synopsis:

This postmarket surveillance study will evaluate the ongoing safety of the Happiest Baby, Inc. SNOO Smart Sleeper in accordance with the order issued under Section 522 of the Federal Food, Drug, and Cosmetic Act, issued March 30, 2023

The study will measure rates of adverse events occurring in the SNOO bassinet from a prospectively screened cohort of 1000 infants determined to be at high risk for SUID. The primary endpoints quantify device-related serious injury and/or device-related death. The secondary endpoints include an analysis of SNOO usage patterns in the enrolled population, including infant age during SNOO use, duration of SNOO use, and weaning rationale.

Procedures:

Prospective participants who have purchased or rented SNOO during the study enrollment period will be invited to participate in an electronic eligibility screening survey 1-month after their purchase/rental ship date. Eligible participants will subsequently be invited to participate in a 6-month follow up survey (7 months after their purchase/rental ship date, 6 months post-enrollment) soliciting self-reported outcomes for the study endpoints. The screening and survey questionnaires will be conducted electronically via Qualtrics using a link provided by email, and which may be completed on a smart phone, tablet, or computer.

As enrolled eligible participants complete their final surveys, responses indicating the occurrence of adverse events will be investigated, classified according to severity and device-relatedness, documented, and reported. A final clinical evaluation of the observed SUID rate will be conducted, and will include reference to demographically-matched population statistics pulled from the CDC WONDER database. A full characterization of adverse events and any demographic or usage-related correlates will be reported to the FDA as part of this investigation.

Interventions

  • Device SNOO Bassinet
    This is a non-interventional, prospective observational and descriptive active surveillance study of a cohort of individuals who have purchased or rented a SNOO for use with their infant.

Primary outcome measures

  • Serious Injury [Time frame: when infant was 0-6 months old (and still using SNOO)]
  • Infant death [Time frame: when infant was 0-6 months old (and still using SNOO)]
Secondary outcome measures (3)
  • Infant age during SNOO use [Time frame: when infant was 0-6 months old (and still using SNOO)]
  • Degree of SNOO use [Time frame: when infant was 0-6 months old (and still using SNOO)]
  • Weaning rationale [Time frame: when infant was 0-6 months old (and still using SNOO)]

Eligibility criteria

Inclusion criteria

Infant/caregiver dyads meeting the following inclusion criteria will be eligible for study enrollment:

  • Respondent must identify as a primary caregiver of the infant.
  • Purchase or rental of SNOO shipped to a U.S. residence during the defined enrollment period.
  • Caregivers must be English speakers ages 18 or older residing in the United States.
  • Infants must use SNOO during the intended use period (i.e., birth to 6 months).
  • Infants must meet at least one of the following criteria for high risk for SUID:
  • Infant race: Black or African American; and/or American Indian or Alaskan Native
  • Maternal education: 12 years or less
  • Low birth weight: <5 pounds 8 ounces (<2500 grams)
  • Last menstrual cycle (LMP) or obstetrical estimate (OE) Gestational age at time of birth: <37 weeks (preterm)
  • Maternal age at time of birth: <25 years
  • Smoking status: Any self-reported maternal smoking during pregnancy

Exclusion criteria

  • Not primary caregiver
  • Does not speak English
  • Is not a US resident
  • Is not 18 years old or older
  • Infant did not use SNOO during the intended use period (i.e., birth to 6 months).
  • Infants does NOT meet at least one of the below risk criteria:
  • Infant race: Black or African American; and/or American Indian or Alaskan Native
  • Maternal education: 12 years or less
  • Low birth weight: <5 pounds 8 ounces (<2500 grams)
  • LMP or OE Gestational age at time of birth: <37 weeks (preterm)
  • Maternal age at time of birth: <25 years
  • Smoking status: Any self-reported maternal smoking during pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Happiest Baby, Inc. — Los Angeles

Identifiers

NCT: NCT06361303 · PS230001 · PS230001 / PSS001

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗