Actively Recruiting
Exactech Hip Systems Post-Market Clinical Follow-up (PMCF)
Led by Exactech · Updated on 2024-06-18
2946
Participants Needed
1
Research Sites
689 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A Post-Market Domestic (US) and International Data Collection to Assess Exactech Hip Systems
CONDITIONS
Official Title
Exactech Hip Systems Post-Market Clinical Follow-up (PMCF)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must be 18 years of age or older.
- Participants must be willing and able to provide written informed consent.
- Participants must be receiving or have received an Exactech Hip System total hip arthroplasty for any approved use.
- The hip replacement surgery must be performed by the investigator or a surgeon sub-investigator.
- Devices must be used according to approved indications.
- For participants with prior surgery, sufficient pre-operative, operative, and postoperative data related to the Exactech Hip System must be available in medical records.
- Participants can be newly receiving surgery or enrolled after surgery, with data collected retrospectively and/or prospectively.
You will not qualify if you...
- Participants under 18 years of age at the time of surgery.
- Participants who do not meet the approved population criteria for device use.
- Participants who are pregnant.
- Participants who are prisoners.
- Participants with physical or mental conditions that would invalidate study results.
- Participants who have contraindications for the surgery, such as metal allergy.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tulsa Bone & Joint Associates
Tulsa, Oklahoma, United States, 74146
Actively Recruiting
Research Team
P
Pearl Harris
CONTACT
A
Alex Knisely
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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