Study on Effective Mydriasis in Premature Infants

Key facts

Sponsor

Georgetown University

Principal Investigator

Monisha Bahri, MD

Georgetown University Hospital

Intervention

1% phenylephrine and 0.2% cyclopentolate(drug)

Enrollment

15 enrolled

Eligibility

All sexes

Timeline

2007 – 2008

Study locations (1)

• Georgetown University Hospital, Washington D.C., District of Columbia, United States

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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