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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03377205
Other study ID # 2016/137 (REK)
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date June 2016
Est. completion date January 2026

Study information

Verified date July 2023
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to make a survey of functional outcome, radiological outcome and complication rate after intramedullary nailing (IMN) and plate fixation of Weber B ankle fractures in elderly patients, and contribute in choosing the best surgical method for these ankle fractures.


Description:

Open reduction and internal fixation (ORIF) is the gold standard treatment for unstable Weber B fractures, using compression screws and a neutralization plate. In the elderly, pre-existing co-morbidities, osteoporosis and poor skin conditions may give a high complication rate, including wound complications, symptomatic hardware and hardware failure. Due to concerns with complications related to ORIF, the technique with intramedullary fixation has been introduced. This method may simplify the management when poor skin conditions and osteoporotic bone, and has the potential to reduce the risk of soft tissue and hardware complications. Previous studies have showed that intramedullary fixation is probably the best choice for treating unstable ankle fractures in elderly patients, but more studies are needed to conclude the superiority to standard plate fixation.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 120
Est. completion date January 2026
Est. primary completion date June 2021
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: - Acute unstable Weber B fracture (unimalleolar, bimalleolar or trimalleolar fractures). - Operable with both methods of surgery within 3 weeks after injury. - Men and women = 60 yoa. Exclusion Criteria: - Prior injury or pathology with reduced ankle function. - Other acute foot/ankle/leg injury that will affect ankle function. - Fracture of the posterior malleolus that need fixation. - Injury / pathology that may affect rehabilitation. - Open fracture. - Inoperable patient. - Dementia (MMSE score = 24 points), reduced competent to consent, not able to express himself/herself in Norwegian or English.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Compression screws and neutralization plate
Open reduction and internal fixation with screws and plate
Acumed Fibular Rod System
intramedullary nailing of fibula

Locations

Country Name City State
Norway Oslo University Hospital Oslo

Sponsors (3)

Lead Sponsor Collaborator
Oslo University Hospital Ostfold Hospital Trust, Vestre Viken Hospital Trust

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary American Orthopaedic Foot and Ankle Society (AOFAS) score Functional outcome as assessed by AOFAS score (0-100) 5 years
Secondary Manchester-Oxford Foot questionnaire (MOxFQ) Patient reported outcome as assessed by MOxFQ (0-100) 5 years
Secondary Olerud and Molander Score (OMS) Patient reported outcome as assessed by OMS (0-100) 5 years
Secondary EuroQol-5d (Eq-5d) Patient reported quality of life as assessed by Eq-5d index score 5 years
Secondary Visual analogue scale (VAS) VAS scores for pain during rest (0-10), during walking (0-10), at night (0-10), and during daily activities (0-10), where 10 is best 5 years
Secondary Fracture reduction as assessed by CT scans Number of patients with good, fair or poor fracture reduction 3 months
Secondary Malunion as assessed by CT scans Number of patients with malunion 5 years
Secondary Nonunion as assessed by CT scans Number of patients with nonunion 5 years
Secondary Osteoarthritis as assessed by CT scans Number of patients with osteoarthritis assessed according to the criteria by McLennan et al 5 years
Secondary Infection Number of patients with wound infection or deep infection 3 months
Secondary Delayed wound healing Number of patients with delayed wound healing 3 months
Secondary Other complications Number of patients with other complications (e.g. hardware complications, tromboemolism, neurologic complications, peroneus tendon irritation) 5 years
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