Clinical Trials Directory

Trials / Completed

CompletedNCT03528915

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

Conjunctivitis Incidence in the Newborn Within the First Week of Life: Impact of the Prophylactic Use of Rifamycine(CRY NOT).

Status
Completed
Phase
Study type
Observational
Enrollment
881 (actual)
Sponsor
Centre Hospitalier Universitaire, Amiens · Academic / Other
Sex
All
Age
36 Weeks – 36 Weeks
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
OTHERRifamycine treatmentPhone prospecting: occurrence of conjunctivitis in newborns treated with rifamycine treatment in delivery room.
OTHERwhithout Rifamycine treatmentPhone prospecting: occurrence of conjunctivitis in newborns did not receive eye drop treatment in delivery room according to new guidelines.

Timeline

Start date
2015-09-09
Primary completion
2016-05-12
Completion
2016-07-24
First posted
2018-05-18
Last updated
2019-01-23

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03528915. Inclusion in this directory is not an endorsement.