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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04372251
Other study ID # 20/00912
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 5, 2020
Est. completion date December 2031

Study information

Verified date April 2022
Source Ostfold Hospital Trust
Contact Wolfram Grün, MD
Phone +4741297874
Email wolframgruen@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this randomized controlled trial, the outcomes of two surgical techniques for intraarticular calcaneal fractures will be evaluated and compared.


Description:

Operative treatment of calcaneal features through an extensile lateral approach (ELA) has been the gold standard over many years despite high rates of infection and soft tissue complications. Lately, there has been a trend towards less invasive fixation methods. Minimally invasive plate osteosynthesis using the sinus tarsi approach (STA) has gained popularity during the last decade. Furthermore, percutaneous reduction and fixation techniques have been described and used for a few decades. In the early 2000s, Rammelt et al. were the first who introduced a percutaneous technique assisted by hindfoot arthroscopy. The percutaneous and arthroscopically assisted calcaneal osteosynthesis (PACO) is applicable in Sanders II and III fractures and has been shown to provide good clinical outcomes as well as a low rate of complications. The study is designed as a superiority study. Our hypothesis is that the percutaneous and arthroscopically assisted technique provides superior outcomes compared to the sinus tarsi approach in Sanders II and III calcaneal fractures.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date December 2031
Est. primary completion date December 2030
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Dislocated intraarticular calcaneal fracture, type Sanders II or Sanders III with an intraarticular step > 2mm - Patients between 18 and 70 years of age - Acute presentation at one of our departments, enabling surgery within 10 days after injury Exclusion Criteria: - Intraarticular step of < 2mm - Sanders IV fractures - Open fractures - Bilateral injuries - Concomitant major injuries of the foot, ankle or leg that affect the rehabilitation process - Multitraumized patients - Previous injury or surgery of the hindfoot - Charcot foot - Serious medical condition that contradicts surgery - Noncompliant patients - Insufficient Norwegian or English language skills - Patients not available for follow-up - Inability to conduct the rehabilitation protocol

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Sinus tarsi approach (STA)
Osteosynthesis
Percutaneous Arthroscopically Assisted Osteosynthesis (PACO)
Osteosynthesis

Locations

Country Name City State
Norway Haukeland University Hospital Bergen
Norway Vestre Viken Hospital Trust - Drammen hospital Drammen
Norway Oslo university hospial Oslo
Norway Vestre Viken Hospital Trust - Bærum hospital Sandvika
Norway Østfold Hospital Trust Sarpsborg Østfold

Sponsors (4)

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

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Manchester-Oxford Foot Questionnaire (MOxFQ) Foot-Ankle specific PROM (0-100 with 0 representing the best possible outcome) 5 years
Secondary American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot score Widely used foot/ankle score (0-100 with 100 representing the best possible outcome) 5 years
Secondary Calcaneus Fracture Scoring System (CFSS) Calcaneal fracture specific scoring system (0-100 with 100 representing the best possible outcome) 5 years
Secondary Self-reported foot and ankle score (SEFAS) Foot-Ankle specific PROM (0-48 with 48 representing the best possible outcome) 5 years
Secondary Visual Analogue Scale (VAS) for pain Scores pain at rest and on activity (0-10 with 0 representing no pain) 5 years
Secondary Incidence of complications Yes/no for deep or superficial infection, nerve or tendon injury, deep venous thrombosis, hardware complaints and secondary surgery 5 years
Secondary Böhler angle Böhler angle pre- and post surgery as well as at follow up 5 years
Secondary Subtalar osteoarthritis The presence of subtalar osteoarthritis is graded based CT scans taken at the 2 year and 5 year follow-up using the Kellgren & Lawrence classification system. 5 years
Secondary EQ-5D-5L Measure of health-related quality of life. This will be evaluated at the 2-year and 5 -year follow-up. 5 years
See also
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