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Pain Detection and Interception in Neonates

Pain Detection and Interception in Neonates During Blood Sampling

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00447824
Enrollment
160
Registered
2007-03-15
Start date
2007-03-31
Completion date
2009-11-30
Last updated
2007-03-15

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

Conditions

Pain Detection, Pain Intervention

Keywords

Pain, Neonates, NIDCAP, Venous, Capillary

Brief summary

Hypothesis: 1. May the introduction of NIDCAP during blood sample reduced pain in neonates during blood sample 2. Compare the effect of venous and capillary blood sample method

Detailed description

introducing the: Newborn Individualized Developmental Care and Assessment Program

Interventions

PROCEDUREIntroduction of better conditions during blood sampling

Sponsors

Helse sor
CollaboratorUNKNOWN
Sorlandet Hospital HF
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
31 Weeks to 36 Weeks
Healthy volunteers
Yes

Inclusion criteria

* Born gestation age 31-36

Exclusion criteria

* Infection, respiratory distress

Design outcomes

Primary

MeasureTime frame
value of Premature Infant Pain Profile
Heart rate
Saturation
Skin conductance changes

Countries

Norway

Contacts

Primary ContactKnut G Hernes, Dr
drhernes@gmail.com+(47) 957 99999

Outcome results

None listed

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