This prospective, randomized study was conducted to compare the clinical outcomes of the
modified Brostrom procedure using a suture anchor and bone tunnel for chronic lateral ankle
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Full eligibility criteria for NCT01056055
Ages eligible for Study
15 Years to 44 Years
Genders eligible for Study
Accepts Healthy Volunteers
Patients who complained of subjective instability of the ankle joint in whom repeated sprain injuries for > 6 months and pain were confirmed
Patients with marked ankle instability confirmed by the anterior drawer test as compared with the contralateral ankle joint and tenderness involving the lateral ligament of the ankle joint was confirmed on physical examination
Patients with an talar tilt angle exceeding 10o or a discrepancy of > 5o as compared with the non-affected side on stress radiography
Patients with an anterior talar translation exceeding 10 mm or a discrepancy > 3 mm as compared with the non-affected side.
Patients who concurrently had an ankle fracture or marked tendon damage were excluded from the current analysis.
All locations for NCT01056055
Korea, Republic of (1)
Chungbuk National University Hospital
Cheongju, ChungBuk, Korea, Republic of, 360-711
View full eligibility
Tris trial is registered with FDA with number: NCT01056055. The sponsor of the trial is Chonbuk National University Hospital and it is looking for 40 volunteers for the current phase.
Official trial title: Outcomes of the Modified-Brostrom Procedure Using Suture Anchor for Chronic Lateral Ankle Instability - A Prospective, Randomized Comparison With the Bone Tunnel Technique
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