Autopsy report · NCT04563299
Effect on Pain and Inflammation With DEXTENZA Treatment in Patients Undergoing Intravitreal Anti-VEGF Injections
Cause of deathSlow enrollment
“Subject Enrollment”
Life of this trial
- Registered 3 months before it started.
- Ran for about 2 years 2 months before it stopped.
- 10 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Retina Vitreous Associates of Florida
- Sponsor type
- University, hospital or other
- Conditions
- Neovascular Age-related Macular Degeneration; Diabetic Macular Edema; Retinal Vein Occlusion
- Interventions
- Dextenza 0.4Mg Ophthalmic Insert; Prednisolone Acetate
- Participants
- 10
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Safety Study of Autologous Cultured Adipose -Derived Stem Cells for the Fecal Incontinence
“Few subject enrolled” - AccuLIF® PROSPECTIVE PATIENT OUTCOMES STUDY
“Lack of subject enrollment” - Effectiveness Study of Santyl Ointment to Treat Pressure Ulcers
“Low enrollment of qualified subjects” - Efficacy and Tolerability of Ramelteon in Patients With Rapid Eye Movement (REM) Behavior Disorder and Parkinsonism
“Low subject recruitment and enrollment.” - The Impact of Salmeterol-Fluticasone on Sleep in Patients With COPD
“Study subject enrollment difficulties”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.