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Antifibrinolytic Agent
Tranexamic acid injection for Swelling
Phase 4
Waitlist Available
Research Sponsored by Consultants in Ophthalmic and Facial Plastics Surgery
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2nd post op visit: post-op day 7 to 10
Awards & highlights
Study Summary
This study is evaluating whether TXA can reduce post-operative bruising.
Eligible Conditions
- Swelling
- Bruising
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2nd post op visit: post-op day 7 to 10
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2nd post op visit: post-op day 7 to 10
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Post-operative edema/ecchymosis
Secondary outcome measures
Post-operative complications
Side effects data
From 2021 Phase 3 trial • 1226 Patients • NCT047331575%
Vomiting
2%
Dizziness
1%
Nausea
100%
80%
60%
40%
20%
0%
Study treatment Arm
Study Group/Group A_(Tranexamic Acid)
Control Group/Group B_(Placebo)
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Tranexamic acid armExperimental Treatment1 Intervention
Eyelid(s) that received tranexamic acid in the local anesthetic
Group II: ControlActive Control1 Intervention
Eyelid(s) that receive local anesthetic without tranexamic acid
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tranexamic acid
FDA approved
Find a Location
Who is running the clinical trial?
Consultants in Ophthalmic and Facial Plastics SurgeryLead Sponsor
Frequently Asked Questions
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