Amphia Premature Infant Pain Study

Premature Infant Clinical Trial

— APIP  

Official title:

Amphia Premature Infant Pain Study; Breast Milk vs Sucrose

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01276366
• Other study ID #: NL30111.101.09
• Status: Completed
• Phase: N/A
• Start date: January 1, 2010
• Est. completion date: April 1, 2012

Study information

• Verified date: January 2019
• Source: Amphia Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Last thirty years, many research was performed concerning pain in the newborn. These investigations showed us the negative effects of pain in the neonatal period. Our research concerns the choice of analgesics for the premature newborn during a heel lance. Newborns with a gestational age of 32-37 weeks are randomly assigned over three groups. They can receive breastfeeding, during the heel lance, a bottle with supplemental breast milk or sucrose.

The primary objective of the Amphia Premature Infant Pain study, is to investigate whether there is a difference in PIPP-scores in premature newborns who undergo a heel lance, receiving breast milk or sucrose. Our hypothesis is that the PIPP-score will be lower in newborns receiving breast milk compared to sucrose. And the investigators presume that breast feeding has the same analgesic effect as giving supplemental breast milk.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 75
• Est. completion date: April 1, 2012
• Est. primary completion date: August 1, 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A to 2 Months

Eligibility

Inclusion Criteria:

• born at a gestational age between 32+0 and 36+6 weeks,

• being nourished with breast milk

• the necessity for a clinical blood sample.

Exclusion Criteria:

• perinatal asphyxia,

• birth trauma,

• condition of cardio-respiratory instability,

• condition of serious nutritional problems with clinical evidence of gastro oesophageal reflux disease,

• drug abuse of the mother

• and application of sedative medication to mother or child.

Related Conditions & MeSH terms

• Breast Feeding, Exclusive
• Premature Birth
• Premature Infant
• Puncture Skin

Intervention

Other:
• breast feeding
Newborns who are assigned to group one, receive breastfeeding during the blood sample and thereby have skin-skin contact between mother and child.
• supplemental breast milk
In group two, the newborns receive supplemental breast milk, lying in the arms of a nurse during the heel lance.
• sucrose
In the third group, newborns receive sucrose 1ml 24% two minutes before procedure, followed by non-nutritive sucking. During the procedure the newborn lies in his cot.

Locations

Country	Name	City	State
Netherlands	Amphia Hospital	Breda	Noord Brabant

Sponsors (1)

Lead Sponsor	Collaborator
Amphia Hospital

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain scores assessed by the PIPP score	The primary outcome in this trial is the PIPP-score.The PIPP-score is a multidimensional pain assessment measure developed in 1995 . The PIPP-score is validated for procedural and post-operative pain in premature and term newborns.	The PIPP score will be assessed during a heellance. This heellance will be performed after one day of life and before two months.
Secondary	Pain score assessed by the COMFORTneo score	The COMFORTneo is a secondary outcome.The COMFORTneo is a pain assessment measure modified from the COMFORT behaviour scale. In 2009 the COMFORTneo is validated for prolonged pain. The COMFORTneo is not validated for procedural pain yet .	The COMFORTneo score will be assessed during a heellance. This heellance will be performed after one day of life and before two months.
Secondary	partial correlation between the two pain assessment tools.	A secondary outcome is the partial correlation between the PIPP-score and the COMFORTneo score for a heellance in babies born with a postconceptional age between 32 and 37 weeks. When all films are observed, the COMFORTneo scores and PIPP scores are evaluated. We measure a partial correlation coefficient between these scores, to compare these two scores.	up to 2 years
Secondary	intra-class correlation coefficient	This secondary outcome measure gives us information about the uniformity of the assessment of the films between the three investigators.	up to 2 years