Can Immediate Post-injury Fluoxetine Improve the Recovery Trajectories of Victims in Bodily Trauma?
Recruiting
Phase 4
Interventional Study
Musculoskeletal Injury
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 85
- Sex
- Any
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 200 (estimated)
- Sponsor
- University of Florida · Other
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About This Trial
With this prospective double-blinded, placebo controlled clinical trial we hypothesize that immediate (post-injury) intervention with Fluoxetine will prevent/mitigate the development of negative psychiatric symptomology such as PTSD and depression for victims of bodily trauma. We also hypothesize that immediate use of Fluoxetine will decrease subjects' pain, pain interference and opioid use withou…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Admitted to UF Health for trauma resulting in:
* One or more extremity fractures requiring surgery
* Pelvic Fracture
* Chest/abdominal Injury requiring intervention in operating room
* Polytrauma (multiple organ systems/multiple fractures) or Beck Depression Inventory (…
Contacts