Clinical Trials Directory

Trials / Completed

CompletedNCT03497481

Neopterin Dosage in the Eye

Appreciation of the Possibility of Dosing Neopterin in Eye Liquids. Pilot Study of Neopterin Dosage in Eye Liquids.

Status
Completed
Phase
Study type
Observational
Enrollment
20 (actual)
Sponsor
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to determine whether neopterin can be dosed in the fluid of the eye's anterior chamber for patient with non-inflammatory and non-infectious ophthalmic pathology.

Detailed description

The study will be explained to subjects who are about to undergo ophthalmologic surgery. They will sign an informed consent and be included in the study. Urine sample will be collected specifically for the study. Eye's anterior chamber fluid will also be collected during the surgery as it is the usual practice (the sample is used for the neopterin dosage instead of being thrown away). These samples will be centrifuged, frozen in a -80° C freezer. At the end of the study, all the samples will be sent to the central Lab for the neopterin dosage analysis. Results will be communicated to the principal investigator afterward.

Conditions

Interventions

TypeNameDescription
BIOLOGICALSamplesEye's anterior chamber fluid and urines are sampled for posterior neopterin analysis

Timeline

Start date
2018-06-22
Primary completion
2019-01-25
Completion
2019-01-25
First posted
2018-04-13
Last updated
2022-10-26

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03497481. Inclusion in this directory is not an endorsement.

Neopterin Dosage in the Eye (NCT03497481) · Clinical Trials Directory