TrialX
Image

Gas Tamponade for Prevention of Postoperative Vitreous Hemorrhage in Diabetics

Gas Tamponade for Prevention of Postoperative Vitreous Hemorrhage in Diabetics

Recruiting
18-85 years
All
Phase N/A

Overview

Subjects undergo vitreous substitution with either SF6 gas or fluid during vitrectomy.

Description

Hypothesis: Subjects undergoing vitreous substitution with 30% SF6 gas during vitrectomy will have fewer postoperative vitreous hemorrhages compared to control subjects

Randomization: Subjects will be randomized according to a coin toss during PPV: heads undergo 30% SF6 gas tamponade, tails undergo vitreous substitution with fluid

Eligibility

Inclusion

  1. Subject age is 18-85 years.
  2. Subject consents to study participation and is capable of 6 months of follow-up.
  3. The subject has type I or II Diabetes Mellitus with active PDR in the study eye.
  4. Best-corrected spectacle visual acuity (BCSVA) on the Snellen eye chart ranges from 20/40 to hand motions in the study eye.
  5. The subject is determined to need a PPV for the primary indication of VH secondary to PDR. Exclusion
  6. Subject has significant vitreoretinal adhesion (Grades 2 or 3) (i.e. extensive fibrous proliferation or tractional retinal detachment).
  7. Subject is known to have a significant retinal/optic nerve disease otherwise unrelated to Diabetes Mellitus, which in the opinion of the examiner is responsible for two or more lines of reduced BCSVA (macular degeneration, optic neuritis, glaucoma, amblyopia, etc.) in the study eye.
  8. Subject is known to have macular ischemia, which in the opinion of the examiner, is responsible for two or more lines of reduced BCSVA in the study eye.
  9. Subject has a significant corneal or cataract opacity, which in the opinion of the examiner, is responsible for two or more lines of reduced BCSVA (corneal scar, ectasia, etc.) in the study eye.
  10. Subject has had a previous vitrectomy (anterior or PPV) in the study eye.
  11. Subject has uncontrolled neovascular glaucoma (intraocular pressure > 30 mmHg despite medical/surgical treatment) in the study eye.
  12. Subject has uncontrolled hypertension (systolic > 200 mmHg or diastolic > 120 mmHg) despite adherence to a multiple anti-hypertensive medication regimen.

Study details
    Proliferative Diabetic Retinopathy

NCT04380077

Rush Eye Associates

5 August 2020

Step 1 Get in touch with the nearest study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team


Email

View email

Phone

Phone country flag

View phone
Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.