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Pain Detection and Interception in Neonates

NCT00447824 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2007-03-15

No results posted yet for this study

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

Conditions

  • Pain Detection
  • Pain Intervention

Interventions

PROCEDURE

Introduction of better conditions during blood sampling

Sponsors & Collaborators

  • Helse sor

    collaborator UNKNOWN

  • Sorlandet Hospital HF

    lead OTHER_GOV

Principal Investigators

  • Knut G Hernes, Dr

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
31 Weeks
Max Age
36 Weeks
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-03-31
Completion
2009-11-30

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00447824 on ClinicalTrials.gov