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Registration and Treatment of Pain During Eye Examination of Prematurity

NCT01552993 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2016-04-22

No results posted yet for this study

Summary

The aim of this study is to see if paracetamol has a pain-relieving effect during eye examination in premature infants.

Conditions

  • Infant, Premature
  • Retinopathy

Interventions

DRUG

paracetamol

Paracetamol mixture 20 mg/kg + pacifier and glucose

DRUG

sucrose

pacifier and sucrose

Sponsors & Collaborators

  • Norwegian University of Science and Technology

    collaborator OTHER

  • St. Olavs Hospital

    lead OTHER

Principal Investigators

  • Hakon Bergseng, PhD · St. Olavs University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
31 Weeks
Max Age
37 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2012-10-31
Completion
2012-10-31

Countries

  • Norway

Study Locations

More Related Trials

Entities

Drugs

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 NCT01552993 on ClinicalTrials.gov