Two- Part Proximal Humerus - Conservative vs Operative

NCT ID: NCT04106674

Last Updated: 2022-10-25

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-10-01
• Study Completion Date: 2034-10-31

Brief Summary

The proximal humerus fracture (PHFs) is the third most common fracture type in the elderly, and represents 5% of the overall fractures. The incidence is increasing. The purpose of the project is to compare surgical and conservative management of two- part PHFs in light of radiological, economical and clinical outcome. Do the participants between 60 and 85 years of age with displaced two-part PHFs fare better or worse after surgery compared to non-operative treatment?

Detailed Description

The study-design is a single center single blinded randomized controlled trial (RCT) with 2 arms. Patients admitted to Akershus University Hospital (Ahus) with a displaced two-part proximal humeral fracture of OTA/ AO group 11A2 or 11A3 in need of surgical treatment will be randomly allocated to two groups; conservative/ non-operative treatment or open reduction and internal fixation (ORIF).

All following aims evaluated at controls at 6, 12, 26 and 52 weeks. The 6 months and 1 year controls will additionally be conducted by independent physiotherapists. The other controls are conducted by the treating surgeons. The physiotherapists will be blinded of chosen treatment, the patients wearing a t-shirt covering the shoulder at the consultations, hence single blinded RCT.

Primary aim: Functional outcome as evaluated by the Quick DASH (Disability of the arm, shoulder and hand) score at controls.

Preoperative evaluation:

The project participants will supervise and evaluate the data. General history, including; mechanism of injury, occupation, pre-existing medical conditions and medication, smoking history, American Society of Anesthesiologists Classification (ASA classification), BMI, hand dominance. At inclusion, the patient will be asked to fill out quick-Dash, Visual Analog scale (VAS), EQ-5D to determine the baseline-characteristics.

Postoperative evaluation:

Evaluation of postoperative radiographs for reduction of fracture and possible errors of the operative technique by the project participants and a radiologist.

Secondary aims:

1. Initial radiographic examination with standardized radiograph projections; true anterio-posterior projection and scapula projection pre- and post-operative. Registration of radiological complications defined by a reduction of Head-Shaft-Angle (HSA) of ≥10⁰ in frontal plane, screw penetration/cut-out, screw failure or failure of the osteosynthesis on radiographs. Evaluation of fracture healing/ non-union.

2. Evaluation of postoperative reduction: Reduction of tubercles, rotation of caput, re-establishment of medial support, position of calcar screws and distance from screws to cartilage in x-rays. Computer-tomographic scans are standard pre-operative practice at our institution. The problem of intra- and inter-observer reproducibility is a well-known confounder of fracture classification in proximal humeral fractures and CT scans will help clarify classification (19, 20) and fracture configuration. CT scan postoperatively will be taken within few days after surgery (Only in Stratum 1).

3. Qualitative Computed Tomography (QCT) is an alternative method to measure Bone Marrow Density (BMD) using a Hydroxyapatite plate/ a phantom. This is a flat plate placed under the shoulder during ordinary CT scanning. Several studies have demonstrated an association between the QCT measurements and risk of fragility fractures, so BMD will be assessed.

4. Functional outcome of surgical treatment as evaluated by Constant score by independent physiotherapists during follow-up. Measurement of strength according to recommendations given by the European Society of Shoulder and Elbow Surgeons ESSSE (http://secec.org/).

5. Functional outcome evaluated by Oxford Shoulder score, which is a validated patient-reported outcome measure. A shoulder-specific instrument designed to assess the outcome of all shoulder surgeries.

6. EQ-5D, a generic measure of health status that provide a simple descriptive profile used in clinical evaluation of health care. EQ-5D is recommended for use in cost-effectiveness in Health and Medicine and by the Washington panel of Pharmacoeconomics and outcomes research (ISPOR) task.

7. Health economic registration; length of hospital-stay, sick leaves, use of physiotherapy, appointments at general practitioners, extra controls at in-patient orthopedic clinic, removal of plate or nail, extra surgeries.

8. Monitoring complications such as deep or superficial infection, reoperations, avascular necrosis, non-union, nerve or vessel-damage.

In the literature, the following risk factors for failure of the osteosynthesis, Avascular necrosis (AVN) or chance of poor functional outcome are outlined; the factors will be examined as subgroups to see whether they are representative also for our population:

• A non-adequately reduced fracture. Evaluated in postoperative radiographs. Malalignment?
• Not adequately positioning of implant
• Degree of medial comminution and medial hinge (the amount of metaphyseal bone attached to the anatomic head fragment at trauma.
• Is sufficient medial support achieved in our patients, and if not, does the construction fail?
• Varus subsidence, measured as reduced Head shaft angle (HSA) (>10 degrees) during follow up
• Fixation in varus, HSA <120 or HSA <110 .
• Enough contact between head and shaft for healing?
• Age: Increasing age predisposes osteosynthesis failure and reduced function, probably because of decreasing bone density in proximal humerus in older age. The examiners want to examine whether there is a cut-off in age, in example 60, 65, 75, 80 or 85 years of age.
• Valgus >45 or Varus <30, which fracture is the worst?

Patients allocated to the conservative group may be offered surgical treatment if the fracture changes/ dislocates, in example no contact between the fracture ends if the patients activities of daily living (ADL) is greatly affected or pain is disproportionately

Conditions

Proximal Humerus Fracture; 2 Part Fracture

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Non-surgical

No surgery

Group Type: NO_INTERVENTION

No interventions assigned to this group

Surgical

Surgeons preference

Group Type: ACTIVE_COMPARATOR

Open reduction internal stabilisation (ORIF)

Intervention Type: PROCEDURE

Treatment allocated to surgical or non-surgical group. Implant choice pragmatic, surgeons choice.

Interventions

Open reduction internal stabilisation (ORIF)

Treatment allocated to surgical or non-surgical group. Implant choice pragmatic, surgeons choice.

Intervention Type: PROCEDURE

Other Intervention Names

Surgery

Eligibility Criteria

Inclusion Criteria

1. Patients > 60 years and <85 years

2. More than 50% displacement between head or shaft or 50⁰ angulation of the head against the shaft in Y-projection or more than 45 ˚ valgus or more than 30˚ varus of the Head Shaft Angle (HSA).

3. Patient with tuberculum majus or minor fractures which displaced <5mm can be included as long as points 1 and 2 above are fulfilled.

Exclusion Criteria

• Refusal to participate in the study
• Fracture more than 3 weeks old
• No contact btw head and shaft
• Ipsilateral damage that will influence the recovery and scoring systems
• Incapability to protect osteosynthesis, i.e. use of crutches because of injury to lower extremity. This is up to the treating surgeon to decide
• Pathological fracture or previous fracture of the same proximal humerus
• Multitrauma or "multifractured patient"
• Neurovascular injury
• Open fracture
• Noncompliance, dementia and/ or institutionalized
• Congenital anomaly
• Ongoing infectious process around the incision site for osteosynthesis
• Systemic disease that may influence healing processes or scoring systems (in example Rheumatoid arthritis/Multiple sclerosis/ poorly controlled DM)
• Fracture dislocation
• Substance abuse
• Inability to read and understand Norwegian
• Patients not residing in our catchment area
• Patients with a diameter of the humerus to small for nailing, will be allocated to the Philos-group.
• Any medical condition that excludes surgical treatment, including patients with ASA 3 or 4 that are considered too ill to go through surgery.

• Minimum Eligible Age: 60 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University Hospital, Akershus

OTHER

Sponsor Role: lead

Responsible Party

Hendrik Frolich Fuglesang

Consultant, Head of orthopedic trauma unit

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Asbjørn Aarøen, Professor

Role: STUDY_DIRECTOR

Akershus Universitetssykehus HF

Locations

Akershus University Hospital

Lørenskog, Oslo County, Norway

Site Status: RECRUITING

Countries

Norway

Central Contacts

Annette Konstanse Bordewich Wikerøy, MD

Role: CONTACT

awikeroy@hotmail.com

004799717481

Hendrik Fuglesang, MD, PhD

Role: CONTACT

drhendrik@me.com

Facility Contacts

Per-Henrik Randsborg, PhD MD

Role: primary

pran@ahus.no

+4797040480

Asbjørn Årøen, PhD MD

Role: backup

asbjorn.aroen@uio.no

+4791587140

References

Handoll HH, Elliott J, Thillemann TM, Aluko P, Brorson S. Interventions for treating proximal humeral fractures in adults. Cochrane Database Syst Rev. 2022 Jun 21;6(6):CD000434. doi: 10.1002/14651858.CD000434.pub5.

Reference Type: DERIVED

PMID: 35727196 (View on PubMed)

Other Identifiers

2018/1583

Identifier Type: -

Identifier Source: org_study_id