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Clinical Trials/ACTRN12612001257853
ACTRN12612001257853CompletedPhase 2

Red light (670nm) treatment to prevent retinopathy of prematurity (ROP)

Canberra Hospital0 sites25 target enrollmentStarted: November 29, 2012Last updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
25

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Non-randomised trial
Primary Purpose
Prevention
Masking
Open (masking not used)

Eligibility Criteria

Ages
24 Weeks to 30 Weeks (—)
Sex
All

Inclusion Criteria

  • Premature neonates less than 30 weeks gestation or less than 1150 grams birthweight
  • Informed consent obtained in the first 24-48 hours of life

Exclusion Criteria

  • Significant chromosomal or congenital anomalies

Investigators

Sponsor
Canberra Hospital

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