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NCT03528915: CRY-NOT

Prevalence of Conjunctivitis and Indentification of Risk Factors With and Without Prophylactic Antibiotic Treatment in Neonates

Completed Last updated 23 January 2019
What this trial tests

trial testing Rifamycine treatment in Ophthalmia Neonatorum in 881 participants. Completed in 24 July 2016.

Timeline
9 September 2015
Primary endpoint
12 May 2016
24 July 2016

Quick facts

Lead sponsorCentre Hospitalier Universitaire, Amiens
StatusCompleted
Study typeOBSERVATIONAL
Enrollment881
Start date9 September 2015
Primary completion12 May 2016
Estimated completion24 July 2016
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Centre Hospitalier Universitaire, Amiens

Who can join

Adults 36 Weeks to 36 Weeks, any sex, with Ophthalmia Neonatorum. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The French guidelines for the use of Rifamycine eye drops in delivery room to prevent neonatal conjunctivitis have been actualized. Only newborns exposed to risk factors of conjunctivitis should be treated, compared to previous guidelines, treating all newborns. currently, there are no data describing risk factors for neonatal conjunctivitis. This study evaluated the incidence of conjunctivitis with or without Rifamycine eye drops treatment in the delivery room. Then risk factors for neonatal conjunctivitis where analyzed.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Centre Hospitalier Universitaire, Amiens trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03528915.

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