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RecruitingNCT05851898

Pilot study of duloxetine and depressive symptoms after fragility fractures

About this titleRead the official source — NCT05851898
Medication studyAges 65+United StatesDepression
The study in practice

Understand this study

Who could participate?

Listed age limits: from 65 years.

Listed locations
Winston-SalemSee all locations and recruitment
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: April 8, 2024
Recruitment status
Recruiting
Enrollment listed in the registry
100
Sponsor
Wake Forest University Health Sciences
Sponsor type
University
Study type
Drug
Intervention type
Drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
Over 65 Years
Official registry ID
NCT05851898
Official title
Show the full official title

The Role of SNRI's in the Prophylaxis of Depression in the First Year Following Lower Extremity Fragility Fractures in Geriatric Patients

Recruitment & locations

Currently recruiting

Winston-Salem

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Wake Forest University Health Sciences, a university.

Does this study involve medication?

Yes. The study involves medication, including Duloxetine 30 mg.

Who can participate?

Listed age limits: from 65 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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