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Effects of Vanilla on Hypoxic Intermittent Events in Premature Infants (Vanilla)

Primary Purpose

Premature Birth, Neonatal Hypoxic Conditions

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Vanilla scent
Sponsored by
Université de Sherbrooke
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Premature Birth focused on measuring Late preterm, Vanilla, Hypoxic intermittent events

Eligibility Criteria

3 Weeks - 4 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants born between 32.0 and 33.6 weeks of gestational age;
  • Postnatal age between 3 and 4 weeks;
  • No current respiratory or ventilatory support;
  • Stable state for at least the last 48 hours;
  • Parental consent to enroll in the study.

Exclusion Criteria:

  • Respiratory diseases other than apnea;
  • Intraventricular hemorrhage grade 3 or 4 OR leukomalacia;
  • Chromosomal abnormality;
  • Congenital malformations which may result in cardiorespiratory or neurodevelopmental abnormality;
  • Clinical deterioration during the study.

Sites / Locations

  • Nicu - Chus

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Vanilla, Then no vanilla night

No vanilla, Then vanilla night

Arm Description

Participants were exposed to vanilla odor (2 mL of 2% vanillin on the bib, close to the face) on the first night (12-hour recording), and not exposed to vanilla on the third night (control night,12-hour recording) No intervention, no recordings were made on the second night

Participants were exposed to the "control" condition on the first night, which consisted of no vanilla odor (12-hour recording), and then exposed to vanilla odor on the third night (2 mL of 2% vanillin on the bib, close to the face;12-hour recording) No intervention, no recordings were made on the second night

Outcomes

Primary Outcome Measures

Desaturation Index
Number per hour of oxygen saturation < 90% for at least 5 seconds

Secondary Outcome Measures

Percentage of Time of Oxygen Saturation Under 90%
Percentage time in overall duration of oxygen saturation under 90%
Percentage of Time of Periodic Breathing
Percent of time of the recording spent in periodic breathing or in apnea. A periodic beathing epoch was defined as a series of 3 episodes or more of apneas lasting at least 3 seconds and separated by less than 20 seconds of normal breathing Apneas were defined as the absence of respiratory movements for at least 20 seconds or for at least 2 breathing cycles with a decrease of at least 3% in SpO2
Time in Apnea
Percent of time of the recording spent in apnea
Mean SpO2
Mean value of oxygen saturation (%)

Full Information

First Posted
December 4, 2015
Last Updated
August 29, 2022
Sponsor
Université de Sherbrooke
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1. Study Identification

Unique Protocol Identification Number
NCT02630147
Brief Title
Effects of Vanilla on Hypoxic Intermittent Events in Premature Infants
Acronym
Vanilla
Official Title
Effects of Vanilla on Hypoxic Intermittent Events in Premature Infants
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
November 2015 (Actual)
Primary Completion Date
June 2019 (Actual)
Study Completion Date
June 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Université de Sherbrooke

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.
Detailed Description
A weekly screening will be done on all new hospitalized infants at the neonatal care unit of the CHUS born between 32.0 and 33.6 weeks of gestational age. At the beginning of their 2nd week in the neonatal care unit, infant's medical record will be consulted for inclusion and exclusion criteria. At this moment, no information will be noted. Then, team research will discuss with neonatologist to have their opinion concerning the inclusion of a patient in the study. If they agree, the doctor or the nurse having a therapeutic link with the infant will ask parents' infant if they agree to meet the research team to discuss about the research project. Once the agreement will be obtained, parents will be approached by a member of the research team. Project will be explained, questions will be answered and consent form will be obtained. When an infant will be enrolled in the study, a code will be attributed to him and a randomization will established the order of the intervention. Option A) night 1: a 12h cardiorespiratory recording with vanilla, night 2: no recording and night 3: a 12h cardiorespiratory recording without vanilla OR Option B): night 1: a 12h cardiorespiratory recording without vanilla, night 2: no recording and night 3: a 12h cardiorespiratory recording recording with vanilla. All data will be entered in a secured database and a double checked will be done by team members to assess the accuracy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature Birth, Neonatal Hypoxic Conditions
Keywords
Late preterm, Vanilla, Hypoxic intermittent events

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vanilla, Then no vanilla night
Arm Type
Experimental
Arm Description
Participants were exposed to vanilla odor (2 mL of 2% vanillin on the bib, close to the face) on the first night (12-hour recording), and not exposed to vanilla on the third night (control night,12-hour recording) No intervention, no recordings were made on the second night
Arm Title
No vanilla, Then vanilla night
Arm Type
Experimental
Arm Description
Participants were exposed to the "control" condition on the first night, which consisted of no vanilla odor (12-hour recording), and then exposed to vanilla odor on the third night (2 mL of 2% vanillin on the bib, close to the face;12-hour recording) No intervention, no recordings were made on the second night
Intervention Type
Other
Intervention Name(s)
Vanilla scent
Intervention Description
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).
Primary Outcome Measure Information:
Title
Desaturation Index
Description
Number per hour of oxygen saturation < 90% for at least 5 seconds
Time Frame
12 hour period of recording on the night 1 and 3 of each participants, in which they are exposed to vanilla or no vanilla odor
Secondary Outcome Measure Information:
Title
Percentage of Time of Oxygen Saturation Under 90%
Description
Percentage time in overall duration of oxygen saturation under 90%
Time Frame
12 hour period of recording on the night 1 and 3 of each participants, in which they are exposed to vanilla or no vanilla odor
Title
Percentage of Time of Periodic Breathing
Description
Percent of time of the recording spent in periodic breathing or in apnea. A periodic beathing epoch was defined as a series of 3 episodes or more of apneas lasting at least 3 seconds and separated by less than 20 seconds of normal breathing Apneas were defined as the absence of respiratory movements for at least 20 seconds or for at least 2 breathing cycles with a decrease of at least 3% in SpO2
Time Frame
12 hour period of recording on the night 1 and 3 of each participants, in which they are exposed to vanilla or no vanilla odor
Title
Time in Apnea
Description
Percent of time of the recording spent in apnea
Time Frame
12 hour period of recording on the night 1 and 3 of each participants, in which they are exposed to vanilla or no vanilla odor
Title
Mean SpO2
Description
Mean value of oxygen saturation (%)
Time Frame
12 hour period of recording on the night 1 and 3 of each participants, in which they are exposed to vanilla or no vanilla odor

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Weeks
Maximum Age & Unit of Time
4 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants born between 30.0 and 34.0 weeks of gestational age; Postnatal age between 3 and 4 weeks; No current respiratory or ventilatory support; Stable state for at least the last 48 hours; Parental consent to enroll in the study. Exclusion Criteria: Respiratory diseases other than apnea; Intraventricular hemorrhage grade 3 or 4 OR leukomalacia; Chromosomal abnormality; Congenital malformations which may result in cardiorespiratory or neurodevelopmental abnormality; Clinical deterioration during the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Paul Praud, MD, PhD
Organizational Affiliation
Université de Sherbrooke
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nicu - Chus
City
Sherbrooke
State/Province
Quebec
ZIP/Postal Code
J1H5N4
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All results will be made available with other researchers on demand, upon reasonable requests
IPD Sharing Time Frame
Available if requested, up to 2023
IPD Sharing Access Criteria
Similar study protocol
Citations:
PubMed Identifier
24211071
Citation
Brockmann PE, Poets A, Poets CF. Reference values for respiratory events in overnight polygraphy from infants aged 1 and 3months. Sleep Med. 2013 Dec;14(12):1323-7. doi: 10.1016/j.sleep.2013.07.016. Epub 2013 Oct 14.
Results Reference
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PubMed Identifier
21502823
Citation
Nunez J, Cristofalo E, McGinley B, Katz R, Glen DR, Gauda E. Temporal association of polysomnographic cardiorespiratory events with GER detected by MII-pH probe in the premature infant at term. J Pediatr Gastroenterol Nutr. 2011 May;52(5):523-31. doi: 10.1097/MPG.0b013e3181fa06d7. Erratum In: J Pediatr Gastroenterol Nutr. 2011 Jun;52(6):787.
Results Reference
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Effects of Vanilla on Hypoxic Intermittent Events in Premature Infants

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