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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02374281
Other study ID # 1308143
Secondary ID 2013-005043-86
Status Completed
Phase Phase 3
First received February 10, 2015
Last updated March 29, 2016
Start date December 2014
Est. completion date April 2015

Study information

Verified date March 2016
Source Centre Hospitalier Universitaire de Saint Etienne
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santéFrance: French Data Protection Authority
Study type Interventional

Clinical Trial Summary

The management of the pain is a constant care concern in neonatal and maternity units. Many studies show an interest in the use of sugar solutions to reduce nociception during painful events in infants. However, these studies are based mainly on behavioral observation of the newborn but intrinsic mechanisms of analgesic power are not clearly understood for sucrose solutions.

Our hypothesis is that the analgesic mechanism of sucrose solutions in infants involves a subcortical reactivity notably by action via the brain stem. To explore the intensity of pain and evaluate the subcortical activity, we will use 1) the analysis of heart rate variability (frequency indices whose HFnu) as a peripheral witness of subcortical functioning of the autonomic nervous system 2) electroacoustic analysis of the intensity of crying baby, 3) a composite pain score (DAN score).


Description:

The investigators want to show that the short term autonomic nervous system (ANS) response, after a nociceptive action in the new-born in maternity depends on whether it is preceded by non-nutritive sucking and / or sucrose administration.


Recruitment information / eligibility

Status Completed
Enrollment 180
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A to 8 Days
Eligibility Inclusion Criteria:

- Healthy Newborn in maternity unit of the Saint-Etienne University Hospital (France), to receive venipuncture for blood tests or neonatal screening test

- Establishing consent form signed by the holder of parental authority

Exclusion Criteria:

- Children suffering from a disease affecting the central nervous system.

- Children treated with paracetamol oral solution (if cephalohematoma for example) or other analgesics (nalbuphine) or sedative, at the time of registration.

- Newborns impregnated with a prepartum maternal analgesia.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Drug:
Glucose sucking

Water sucking

Other:
No sucking


Locations

Country Name City State
France CHU de Saint-Etienne Saint-etienne

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary High frequency normalized index (HFnu) It is a reflect of the RR short term heart rate variability (HRV) in the frequency domain. It is measured with a ECG Holter monitor. From 15 min before the painful care to 15 min after. No
Secondary Low frequency (LF and LFnu), It is another index of RR heart rate variability (HRV) measured with a ECG Holter monitor. From 15 min before the painful care to 15 min after. No
Secondary Scale of hetero-assessment of pain (DAN) The DAN scale is specific to acute pain of the newborn 15 minutes after the painful care No
Secondary Electro acoustical characteristic of crying newborn : Duration An acoustic recording of children's tears will be conducted in parallel with a microphone and dedicated software to study the properties of crying caused by the puncture. Continuous recording begins at least fifteen minutes before the procedure and is kept up to fifteen minutes after the invasive procedure. The child must be quiet. It will be placed in its cocoon to limit environmental stress From 15 min before the painful care to 15 min after. No
Secondary Frequency domain It is another index of RR heart rate variability (HRV) measured with a ECG Holter monitor. From 15 min before the painful care to 15 min after. No
Secondary The time domain (SDNN, SDANN, pNN50). It is another index of RR heart rate variability (HRV) measured with a ECG Holter monitor. From 15 min before the painful care to 15 min after. No
Secondary LF / HF ratio It is another index of RR heart rate variability (HRV) measured with a ECG Holter monitor. From 15 min before the painful care to 15 min after. No
Secondary Electro acoustical characteristic of crying newborn : Frequency An acoustic recording of children's tears will be conducted in parallel with a microphone and dedicated software to study the properties of crying caused by the puncture. Continuous recording begins at least fifteen minutes before the procedure and is kept up to fifteen minutes after the invasive procedure. The child must be quiet. It will be placed in its cocoon to limit environmental stress From 15 min before the painful care to 15 min after. No
Secondary Electro acoustical characteristic of crying newborn : Frequency variations An acoustic recording of children's tears will be conducted in parallel with a microphone and dedicated software to study the properties of crying caused by the puncture. Continuous recording begins at least fifteen minutes before the procedure and is kept up to fifteen minutes after the invasive procedure. The child must be quiet. It will be placed in its cocoon to limit environmental stress From 15 min before the painful care to 15 min after. No
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