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Skin Blood Flow Changes Using Laser Doppler Imager for Assessment of Pain and Analgesia in Newborn Infants

Skin Blood Flow Changes Using Laser Doppler Imager for Assessment of Pain and Analgesia in Newborn Infants

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00694174
Enrollment
56
Registered
2008-06-10
Start date
2005-09-30
Completion date
2007-09-30
Last updated
2008-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Procedural Pain

Keywords

Procedural Pain in Newborn Infants, newborn infant, acute procedural pain, skin blood flow changes, sucrose analgesia, laser doppler imager, neonatal infant pain scale

Brief summary

The purpose of this study is to assess whether an instrument, the Laser Doppler Imager, is able to measure the effect of pain related changes in skin blood flow in newborn infants. The study will also determine whether the use of sucrose (sugar water) when given by mouth has any effect on pain related skin blood flow changes.

Detailed description

During the last 25 years evidence that newborns can experience pain has been increasing. Painful procedures (injections, heel lances, and circumcisions) are part of normal routine newborn care. Studies have demonstrated that newborns have increased sensitivity to pain when compared with older children and adults. Pain assessment and management is an important component in the overall care of the newborn infant and safe, effective analgesics are needed. Pain assessment is complicated by the infants' verbal and cognitive limitations. Heart rate, blood pressure and oxygen saturation are commonly monitored in the nursery in response to pain, yet these parameters are affected by handling, illness, medications, as well as by pain. Skin blood flow has been documented to increase in premature newborns undergoing painful procedures in the Newborn Intensive Care Nursery. In the present study, Laser Doppler Imager technology will be used to define changes in skin blood flow response to heel lance and oral sucrose administration in normal newborn infants.

Interventions

sucrose 24% oral solution 2 ml one time only dose administered by mouth prior to heel lance

DRUGsterile water

sterile water 2 ml single dose to be administered orally one time prior to heel lance

Sponsors

Children's Hospital of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
1 Days to 7 Days
Healthy volunteers
No

Inclusion criteria

* Informed consent from parent or legal guardian. * Term, newborn infant, between 1 and 7 days of age. * Appropriate for gestational age (weight 5th through 95th percentile).

Exclusion criteria

* Small or large for gestational age (weight\<5th or \>95th percentile). * Physical or biochemical abnormalities. * History of maternal drug dependence. * Apgar score \<7 at 5 minutes. * Current use of analgesics.

Design outcomes

Primary

MeasureTime frame
skin blood flow response (perfusion units, PU)immediately prior to heel lance, at heel lance, 5 minutes post heel lance (3 time points)

Secondary

MeasureTime frame
Blood pressure10 minutes prior to heel lance, 5 minutes after heel lance
Respiratory rate10 minutes prior to heel lance, immediatel prior to heel lance, at time of heel lance, 5 minutes post end heel lance
Heart rate10 minutes prior to heel lance, immediately prior to heel lance, at heel lance, 5 minutes post end heel lance
oxygen saturation (SaO2)10 minutes prior to heel lance, immediately prior to heel lance, at time of heel lance, 5 minutes post end heel lance
Neonatal Infant Pain Score10 minutes prior to heel lance, immediately prior to heel lance, at time of heel lance, 5 minutes post end heel lance
axillary temperature10 minutes prior to heel lance, immediately prior to heel lance, at time of heel lance, 5 minutes post end heel lance

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026