Istanbul University Faculty of Medicine
Istanbul, 34093, Turkey (Türkiye)
NCT Number: NCT03228849
This study aims to compare conservative treatment versus a new suture anchor technique for bony mallet finger in 29 patients.
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Interventional
Not applicable
Istanbul, 34093, Turkey (Türkiye)
This study aims to compare conservative treatment versus a new suture anchor technique for bony mallet finger in 29 patients who presented to investigators' clinic between 2013 and 2015. Patients were randomly assigned to conservative or surgical treatment groups. Patients in the conservative group were followed with immobilization with aluminum splint and physical therapy. Patients in the surgical group were treated with investigators' new surgical suture anchor technique and then received physical therapy. The patients were followed for 12 months. Primary study outcomes were extension deficit, days to return to work and DIP flexion.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Suture anchors were used to attach bony fragment. On week 6, patients were then started on physical therapy for 2 weeks.
The injured finger was immobilized in an aluminium splint for 6 weeks. Patients were then started on physical therapy for 2 weeks.
Time frame: 12 months
The inability to actively extend DIP joint to 0 degrees.
Time frame: 12 months
The maximum angle of flexion at DIP joint
Time frame: Starting from the date of the start of treatment until patients returns to work, assessed up to 12 months
Time to return to work
Istanbul University
Other
Conservative Management Equally Effective to New Suture Anchor Technique for Acute Mallet Finger Deformity: A Prospective Randomized Clinical Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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