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Plate Fixation Versus Intramedullary Nailing of 3 and 4 Part Proximal Humerus Fractures

U

University Hospital, Akershus

Status

Active, not recruiting

Conditions

Shoulder Fractures
Humeral Fractures, Proximal

Treatments

Procedure: Multiloc nail
Procedure: Philos plate

Study type

Interventional

Funder types

Other

Identifiers

NCT02944058
2016/626

Details and patient eligibility

About

The purpose of the project is to compare the management of 3 and 4 part proximal humerus fractures (PHF) with an angular stable plate (Philos) with that of an intramedullary nail (Multiloc) in light of complications, radiological, economical, functional and clinical outcome.

Full description

Randomized controlled trial (RCT) from Akershus University Hospital in Norway. Randomization between two implants. The investigators will use deltopectoral or deltoid split as surgical access. All patients will have calcar screws and cuff sutures. When lack of bone for example after decompressing valgus compressed fractures, a bone-substitute might be used in the surgeons preference. Follow up in outpatient clinic at 6, 12, 52 and 104 weeks, but also a 5 year follow up is planned. Postoperative radiographs of both shoulders and CT of operated shoulder will be taken.

Enrollment

79 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients > 18 years
  2. Severe displacement, defined as malposition of at least 45⁰ of angular deviation in valgus or 30⁰ in varus in true frontal projection, regardless of whether the fracture is impacted or not. Fractures with more than 50% displacement of the head against the surgical neck
  3. The greater or lesser tubercles must be fractured in a 3 or 4-part fracture. The degree of displacement is not critical for inclusion.

Exclusion criteria

Exclusion criteria:

  1. Fracture more than 3 weeks' old
  2. Caput humeri just a thin shell or split
  3. Ipsilateral damage that will influence the recovery and scoring systems
  4. Incapability to protect osteosynthesis, i.e. use of crutches because of injury to lower extremity.
  5. Pathological fracture
  6. Neurovascular injury
  7. Open fracture
  8. Noncompliance
  9. Congenital anomaly
  10. Ongoing infectious process around the incision site for plate osteosynthesis
  11. Systemic disease that may influence healing processes or scoring systems (RA/MS)
  12. Fracture dislocation
  13. Substance abuse
  14. Inability to read and understand Norwegian
  15. Patients not residing in our catchment area
  16. Patients with too small humerus diameter to use a nail
  17. Patient not able to commit and understand written consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

79 participants in 2 patient groups

Philos plate
Active Comparator group
Description:
Intervention is surgery with Philos plate
Treatment:
Procedure: Philos plate
Multiloc nail
Active Comparator group
Description:
Intervention is surgery with Multiloc nail
Treatment:
Procedure: Multiloc nail

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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