UnknownNot Applicable

Evaluation of Inflammation of the Anterior Segment by Laser Flashmeter in Patients Having Undergone Surgery of the Posterior Segment (Vitrectomy or Preindentation) During the First Postoperative Year. (FLAVIC)

100 participantsStarted 2018-09

Plain-language summary

Observational study, monocentric, prospective, descriptive and comparative (eye operated vs fellow eye).

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Major patient, * Operation of vitrectomy or preindentation in the ophthalmology department of Rennes University Hospital for one of the following reasons: * Retinal detachment, rhegmatogenous or not * Combined surgery * Membrane peeling * Macular hole * Optically targeted vitrectomy (Terson's syndrome, intravitreous haemorrhage) * Covered by a health insurance system, * Having received information on the protocol and not having expressed opposition to participating in the study Exclusion Criteria: * Vitrectomy for endophthalmitis or posterior uveitis, * Patient with vitreoretinal proliferation (grade B and C), * Pregnant or nursing woman, * Major patient subject to legal protection (safeguard of justice, guardianship, guardianship), person deprived of liberty.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Evolution of the flare value

Timeframe: Changes between baseline (preoperatively) and day 7, month 1, month 2, month 3, month 6, and month 12 measures

Trial details

NCT IDNCT03677700

SponsorRennes University Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-07

Contact for this trial

Dalal ASRI

299284289 dalal.asri@chu-rennes.fr

View on ClinicalTrials.gov More Inflammation Eye trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.