Clinical Outcomes and Complications of Achilles tendon repair with Percutaneous Achilles Repair System Versus Open Technique of Half-mini-Bunnellmethod for Acute Achilles Tendon Ruptures, a prospective, randomized, controlled trial
Not Applicable
- Conditions
- Acute Achilles Tendon Ruptures
- Registration Number
- JPRN-UMIN000033224
- Lead Sponsor
- Teine Keijinkai Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
patients who have uncertain cause patients suffering from both acute Achilles tendon ruptures patients who have history of steroid injection for Achilles tendon patients who have bone fracture besides acute Achilles tendon ruptures patients who have avulsion fracture of calcaneus
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the period to achieve single -legged heel raises
- Secondary Outcome Measures
Name Time Method