EUCTR2010-018737-21-ITActive, not recruitingNot Applicable
Safety and efficacy of treatment with propranolol in newborns suffering from rethinopathy of the preterm: a pilot study - Propranolol and ROP
AZIENDA OSPEDALIERA MEYER0 sitesStarted: April 7, 2010Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •Newborns with gestational age 23-32 weeks with ROP Stadium 2 Zone II-III without plus
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
Exclusion Criteria
- •Generals: congenital cardiovascolar anormalities, renal failure, cerebral hemorrhages.
- •Local: ROP of stadium higher than II
Investigators
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