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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01524965
Other study ID # HUS-272/13/03/02/2010
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 2011
Est. completion date December 2022

Study information

Verified date May 2020
Source University of Helsinki
Contact Tuomas Lähdeoja, MD
Phone +35894711
Email tuomas.lahdeoja@hus.fi
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Open reduction and locking plate osteosynthesis is a commonly used and well-accepted treatment for displaced fractures of the proximal humerus. The shoulders tend to end stiff despite intensive rehabilitation, limiting the function of the upper extremity and decreasing the quality of life. The accepted postoperative mobilisation protocol includes passive exercises until six weeks postoperatively and active range of motion exercises after that. There is good evidence that conservatively treated fractures of the same site heal better and faster if mobilised immediately. The study compares "standard mobilisation" versus "immmediate mobilisation" in a prospective, randomized, controlled trial in order to find the optimal time-frame for physiotherapy to produce best possible results. Outcome measures are assessed at specific time points after the operation and comparisons between groups are made to follow the rate of recovery and end results.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2022
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age 18 years or older

- Surgery can be performed within 10 days of injury

- A dislocated (>1cm or 35 degrees) AO 11-A2, -A3, -B1 or -B2 fracture of the surgical neck of the proximal humerus with a possible fracture of the Tuberculum Majus

Exclusion Criteria:

- Glenohumeral dislocation

- Fracture of the Tuberculum Minus

- Open fracture

- Additional fractures in the shoulder region

- Other injuries requiring surgical treatment

- Clinically significant injury of the brachial plexus or vasculature

- Pathological fracture associated with cancer

- History of a fracture of the clavicle, scapula or humerus, or history of a very significant disease or trauma of the shoulder region (hemiparesis, tumour, osteomyelitis, grave arthrosis etc)

- Rheumatoid Arthritis in the shoulder requiring active treatment

- Reduced co-operation or incapability for independent living (dementia, mental illness, drug- or alcohol abuse etc)

- Unwillingness to accept some of the treatment options.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Immediate mobilisation after locking-plate osteosynthesis
Immediate passive range of motion exercises are begun postoperatively, after 3 weeks, active unloaded mobilisation begins after three weeks and active, loaded use is allowed 6 weeks postoperatively. Surgical procedure is open reduction of the fracture and internal fixation of the fracture using a locking plate using standard deltopectoral approach and AO principles in fracture management.
Standard mobilisation after locking plate osteosynthesis
Immediately postoperatively the arm is held in a sling, active mobilisation of healthy joints and pendel exercises are befun. Passive range of motion exercises of the shoulder are begun 3 weeks postoperatively. Active mobilisation begins after six weeks. Surgical procedure is open reduction of the fracture and internal fixation of the fracture using a locking plate using standard deltopectoral approach and AO principles in fracture management.
Device:
Osteosynthesis with a locking plate (Philos)
Standard open reduction and internal fixation using a deltopectoral approach. Fracture fixation is done using a locking plate (Philos, Synthes) following the AO principles of fracture management.

Locations

Country Name City State
Finland Töölö Hospital, Helsinki University Central Hospital Helsinki

Sponsors (2)

Lead Sponsor Collaborator
University of Helsinki National Institute for Health and Welfare, Finland

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disablities of Arm, Hand and Shoulder Validated patient-reported upper extremity function scale 3 weeks
Primary Disablities of Arm, Hand and Shoulder Validated patient-reported upper extremity function scale 6 weeks
Primary Disablities of Arm, Hand and Shoulder Validated patient-reported upper extremity function scale 3 months
Primary Disablities of Arm, Hand and Shoulder Validated patient-reported upper extremity function scale 6 months
Primary Disablities of Arm, Hand and Shoulder Validated patient-reported upper extremity function scale 1 year
Primary Disablities of Arm, Hand and Shoulder Validated patient-reported upper extremity function scale 2 years
Secondary Constant Score subjective and objective shoulder score 3 weeks, 6 weeks, 3 months, 6 months, 1 year, 2 years
Secondary Simple Shoulder Test (SST) another shoulder score 3 weeks, 6 weeks, 3 months, 6 months, 1 year, 2 years
Secondary Pain in rest and motion (2 different values) Numeric rating scale 0-10 3 weeks, 6 weeks, 3 months, 6 months, 1 year, 2 years
Secondary Subjective satisfaction Patient reported, Numeric Rating Scale 0-10 3 weeks, 6 weeks, 3 months, 6 months, 1 year, 2 years
Secondary Quality of Life Using the 15D instrument 3 weeks, 6 weeks, 3 months, 6 months, 1 year, 2 years
Secondary Complications Complications of surgery and postoperative phase 3 weeks, 6 weeks, 3 months, 6 months, 1 year, 2 years
See also
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Not yet recruiting NCT02467803 - Shoulder Functional Outcomes of Patients With Proximal Humerus Fractures: Comparison of Two Different Treatment Protocol Phase 0
Recruiting NCT05256849 - Treatment of Humeral Fractures With Long PHILOS Plates Using a Modified Technique and Approach Avoids Radial Nerve Palsy
Completed NCT01105832 - Does Teriparatide (rhPTH 1-34) Promote Fracture Healing in Proximal Humeral Fractures? Phase 4