At a glance
ClinicalIndex Comparison RecordN/ACompleted· 32 enrolled
Drug / intervention
Vanilla scentother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Effects of Vanilla on Hypoxic Intermittent Events in Premature Infants
In Brief
A clinical study evaluating Vanilla scent for Premature Birth and Neonatal Hypoxic Conditions. Completed, enrolled 32 participants across 1 site.
Detailed Summary
The purpose of this study is to evaluate the effect of vanilla odor on hypoxic intermittent events in premature infants born between 32.0 and 33.6 weeks of gestational age.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPremature Birth, Neonatal Hypoxic Conditions
CountriesCanada
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartNov 2015
First PostedDec 2015
Primary CompletionJun 2019
TodayJul 2026
First PostedDec 15, 2015
Enrollment StartNov 1, 2015
Primary CompletionJun 1, 2019
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 10.5 years ago
Interventions
Vanilla scentother
A 12-hour continuous recording for monitoring hemoglobin oxygen saturation, electrocardiogram and respiratory movements will be performed while the infant is exposed to vanilla scent (from vanilla solution on the infant's pyjamas).