Postoperative Pain Control Following Vitreoretinal Surgery
Completed · Phase 4
Conditions studied: Retinal Detachment, Proliferative Vitreoretinopathy, Retinoschisis
In brief
The aim of this study is to evaluate if patients receiving a steroid (triamcinolone acetonide) combined with local anesthesia and antibiotic following retina surgery have better postoperative pain control those receiving local anesthesia and antibiotic alone.
Key facts
- Study ID
- NCT01995045
- Run by
- Emory University
- People needed
- 58
- Starts
- 2012-07-01
- Expected to finish
- 2015-12-01
- Last updated by the study team
- 2017-03-21
Who can join
Age: 18 and older, up to 89. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients undergoing vitreoretinal surgery at the Emory Eye Center Ambulatory Surgery Center and Emory University Hospital by retina attending faculty surgeons
You may not qualify if…
- Unable to verbalize level of pain control
- Pediatric patients (<18 years old)
- Glaucoma, ocular hypertension, or glaucoma suspects
- Allergy to local anesthetic
- Pre-existing chronic pain requiring narcotic pain medication
- Drug addiction
- Impaired periorbital sensation (history of herpes simplex, zoster, corneal graft)
Where it is running
- Emory University Eye Center — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
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