Status:

COMPLETED

Changes in Vital Signs and Pupil Diameter Related to Pharmacologic Mydriasis in Premature Infants: A Randomized Double Blind Clinical Study

Lead Sponsor:

University of the Philippines

Conditions:

Retinopathy of Prematurity

Eligibility:

All Genders

1-32 years

Phase:

PHASE4

Brief Summary

Retinopathy of prematurity (ROP) is one of the common anatomic causes of blindness among Filipinos, accounting for 47.7% of the cases. With this retinopathy being preventable and treatable, ROP screen...

Detailed Description

I. Introduction Retinopathy of prematurity (ROP) is one of the common anatomic causes of blindness among Filipinos, accounting for 47.7% of the cases. With this retinopathy being preventable and treat...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • birth weight of less than 1500 g
  • gestational age of 32 weeks or less
  • an unstable clinical course who are believed to be at high risk for Retinopathy of Prematurity, as assessed by their individual attendings
  • Exclusion criteria cited that
  • infants with cardiac abnormalities directly affecting the heart rate and oxygen saturation
  • infants with inotropic medications
  • infants with ventilatory support

Exclusion

    Key Trial Info

    Start Date :

    September 30 2011

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    September 30 2011

    Estimated Enrollment :

    60 Patients enrolled

    Trial Details

    Trial ID

    NCT04838665

    Start Date

    September 30 2011

    End Date

    September 30 2011

    Last Update

    April 9 2021

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