Oral Propranolol for Prevention of Threshold Retinopathy of Prematurity

Recruiting Phase 2 Interventional Study
Retinopathy of Prematurity
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
5 Weeks – 15 Weeks
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Prevention
Participants needed
276 (estimated)
Sponsor
University of Zurich · Other
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About This Trial
Extremely premature infants are at risk of developing a potentially blinding eye disease, called retinopathy of prematurity (ROP). Currently available treatment, consisting of laser surgery or injection of drugs into the eye balls, may prevent most but not all cases of permanent ROP-mediated blindness. Both types of treatment are associated with significant costs and side effects. An orally admin…
Trial Locations
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Eligibility Criteria
Inclusion criteria: * Preterm infant born before 28 week's gestation * Birth weight below 1250 g * At least 5 weeks of age (at randomisation) * PMA 310/7 - 36 6/7 weeks * Ophthalmoscopic evidence of incipient ROP (stage 1 or 2, with or without plus disease in any zone) * Written informed consent by…
Contacts

Dirk Bassler, M.D.

+41 44 255 53 40

dirk.bassler@usz.ch

CONTACT

Christoph Rüegger, M.D.

+41 43 253 98 10

christoph.rueegger@usz.ch

CONTACT