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NCT04380077

Gas Tamponade for Prevention of Postoperative Vitreous Hemorrhage in Diabetics

Status unknown NA Last updated 18 November 2023
What this trial tests

NA trial testing vitrectomy with sulfur hexafluoride gas in Proliferative Diabetic Retinopathy in 150 participants. Status unknown.

Timeline
15 May 2020
Primary endpoint
21 January 2025
21 January 2025

Quick facts

Lead sponsorRush Eye Associates
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment150
Start date15 May 2020
Primary completion21 January 2025
Estimated completion21 January 2025
Sites1 location across Mexico

Drugs / interventions tested

Conditions studied

Sponsor

Rush Eye Associates

Who can join

Adults 18 to 85, any sex, with Proliferative Diabetic Retinopathy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Hypothesis: Patients undergoing pars plana vitrectomy for the indication of diabetic vitreous hemorrhage will have a lower incidence of postoperative vitreous hemorrhaging during the 6-month trial period when vitreous substitution with 20-30% sulfur hexafluoride gas is utilized compared to vitreous substitution with balanced salt solution.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Proliferative Diabetic Retinopathy

Currently open trials in the same condition.

Other Rush Eye Associates trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04380077.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing