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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02304900
Other study ID # PHRI09-PJP / IOL et sommeil
Secondary ID
Status Completed
Phase N/A
First received November 27, 2014
Last updated February 23, 2017
Start date December 2009
Est. completion date December 2012

Study information

Verified date February 2017
Source University Hospital, Tours
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The cataract surgery (550 000 operations per year in France) is to replace the cloudy lens with a refractive implant. Two colors of implants are available: white implants, filtering out ultraviolet and yellow implants, filtering and more blue light. No clinical data are available to assert the superiority of an implant according to its color and the choice is made according to the preference of the surgeon and / or "markets".

It is established in humans that blue light has an important role on the secretion of melanopsin, a key mediator of the circadian cycle. This "clock" regulates most neuroendocrine functions in the nycthémère (sleep, mood, temperature, cortisol, ..). The question of the impact of these neuro endocrine functions of the installation of a blue light filter into the eyes of patients operated thus arises.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date December 2012
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender All
Age group 60 Years to 90 Years
Eligibility Inclusion Criteria:

- female or male subject

- subject between 60 and 90 years old

- Visual acuteness < or = with 2 eyes

- Indication operating of the cataract

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
white implant
st intervention (in the month following the inclusion): Randomization of the color of the implant nd operation (1 to 3 months after the first surgery): Installation of a same color as the first implant operated eye
yellow implant
st intervention (in the month following the inclusion): Randomization of the color of the implant nd operation (1 to 3 months after the first surgery): Installation of a same color as the first implant operated eye

Locations

Country Name City State
France Service d'Ophtalmologie Brest
France Service d'Ophtalmologie, Centre Hospitalier Paul Martinais Loches
France Service d'Ophtalmologie Tours

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Tours

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Variation between before and 2 months after surgery sleep time 2 months
Secondary Variation between before and 2 months after surgery the number of hours of sleep 2 months
Secondary Variation between before and 2 months after surgery of the quality of sleep 2 months
Secondary Variation between before and 2 months after surgery the mood evaluation score 2 months
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