Efficacy of Loteprednol Ointment Following Eyelid Surgery
Withdrawn before enrolling · Not applicable
Conditions studied: Post-operative Healing Following Blepharoplasty and Ptosis Repair
In brief
Inflammation occurs after any type of incisional surgery. This study will evaluate the efficacy of Loteprednol etabonate ointment vs. Soothe ointment (vehicle) for postoperative inflammation after routine eyelid surgery.
Key facts
- Study ID
- NCT01749241
- Run by
- University of California, San Diego
- People needed
- 0
- Starts
- 2012-09-01
- Expected to finish
- 2015-05-01
- Last updated by the study team
- 2019-08-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age > 18 years old
- Scheduled for bilateral eyelid surgery
- Willing and able to return for all study visits
- Willing and able to administer treatments as required
- Understand and sign informed consent approved by UCSD institutional review board
You may not qualify if…
- History of allergy to investigational drug (Loteprednol etabonate) or ingredient in drug including petrolatum
- History of collagen vascular disease and receiving concurrent treatment that could interfere with interpretation of study results
- Concurrent ocular therapy with nonsteroidal anti-inflammatory drugs, mast cell stabilizers, antihistamines, decongestants, immunosuppresants, and systemic or ocular corticosteroids
- History of immunodeficiency
- Prior eyelid or facial surgery
- Prior ocular or orbital trauma
- History of ocular hypertension, steroid responder, or glaucoma
- Pregnancy or lactation
- Uncontrolled systemic disease or significant illness
- Any other condition the investigator believe would pose a significant hazard to the subject if the investigational therapy were initiated
Where it is running
- Shiley Eye Center — La Jolla, California, United States
Full record on ClinicalTrials.gov
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