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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03050073
Other study ID # IRIS
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 18, 2016
Est. completion date December 31, 2016

Study information

Verified date August 2018
Source Groupe Hospitalier Paris Saint Joseph
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

A chinese study shows that chinese population eyes with a primary angle closure have a greater choroidal thickness than normal eyes.The increase of choroidal thickness would be associated to this primary angle closure.


Description:

Usual ophtalmic consultation for glaucoma with primary angle closure


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date December 31, 2016
Est. primary completion date June 30, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age >18 years

- Primary angle closure confirmed by gonioscopy

- interpretable images for choroidal thickness measure

- interpretable images by Ultra Bio Microscopy (UBM)

Exclusion Criteria:

- Acute crisis for angle closure

- Rethinopathy (diabetic or hypertensive)

- Histories of intra-eye surgery

- Great myopia

- Hypermetropia

- retinal pathology

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Groupe Hospitalier Paris Saint Joseph Paris Ile-de-France

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary change of choroidal thickness measurement by Imaging of the fundus oculi (OCT swept source) Day 1 Day 30
See also
  Status Clinical Trial Phase
Not yet recruiting NCT03160690 - Changes in Choroidal Thickness After Non Penetrating Deep Sclerectomy N/A
Completed NCT01610804 - Choroidal Thickness Measurements During Central Serous Chorioretinopathy (CSCR) Treatment N/A