ClinicalTrials.gg
RecruitingNCT01746537ATACUpdated Mar 4, 2026

Analysis of Anterior Chamber Inflammation by Optical Coherence Tomography

An observational study in Uveitis, sponsored by The Cleveland Clinic. Recruiting at 1 site in United States. Per ClinicalTrials.gov, last updated 2026-03-04.

Sponsored by The Cleveland Clinic · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,500
Sex
All
01

Study summary

A prospective, observational, case series investigating the feasibility of utilizing OCT scans of the anterior chamber of eyes with uveitis.

02

Conditions studied

  • Uveitis

Browse trials for

03

In context

Uveitis

299 studies on the registry are indexed under Uveitis; 32 are open to participants now.

This study's planned enrollment of 1,500 is above the median of 107 across 104 observational studies indexed under Uveitis.

Browse Uveitis studies →

Lead sponsor

The Cleveland Clinic is the lead sponsor of 831 studies on the registry; 119 are open to participants now.

Of its 90 completed or terminated interventional studies of FDA-regulated products, 73 (81%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Patients with inactive and active uveitis.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All patients presenting to Cole Eye Institute with uveitis.

Exclusion criteria

Exclusion Criteria:

  • Inability to provide , including non-English speaking and cognitively/mentally impaired.
  • Severe corneal opacities preventing imaging of anterior chamber
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,500 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Use the OCT to objectively image and grade the degree of anterior chamber inflammation in eyes with inactive and active uveitis.

    Time frame: one year

07

Study locations

1 of 1 sites recruiting
  • Cole Eye Institute
    Cleveland, Ohio 44195, United States
    Recruiting
    • Sunil K Srivastava, M.D. · Contact216-636-2286
    • Kimberly M Baynes, BSN,RN · Contact216-444-2566
    • Sunil K Srivastava, M.D. · Principal investigator
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01746537
Responsible party
Sunil Srivastava (Medical Doctor, The Cleveland Clinic) — Principal investigator
First posted
Dec 11, 2012
Start date
Jun 2012
Primary completion
Jun 2028 (estimated)
Completion
Jun 2029 (estimated)
Last update
Mar 4, 2026

Study contacts

Sunil K Srivastava, M.D.
Contact
216-636-2286
Kimberly M Baynes, BSN, RN
Contact
216-44-2566
Sunil K Srivastva, MD
principal investigator · The Cleveland Clinic

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion