Open Reduction and Internal Fixation of Humeral Midshaft Fracture: Anterior Versus Posterior Plate Fixation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16-65
SponsorDr Jahanzaib Ramay

About this trial

About 13 out of 10,000 patients get a humeral shaft fracture each year, accounting for 1.0-3.0% of all fractures. The central part of the humerus is where 60% of all humeral fractures occur. A midshaft humerus fracture typically happens because of a direct impact to the upper arm. Trauma, such as falls, motor vehicle accidents, or motorcycle accidents, is the most common cause of fractures. Internally fixing humeral shaft fractures is often accomplished by a variety of surgical techniques. Usually, the posterior technique is used to repair distal and mid-shaft fractures. However, the posterior technique necessitates lateral or prone stance. The aim of this study comparing the outcomes of internal fixation and open reduction of humeral midshaft fractures utilizing anterior and posterior plate fixation. We want to conduct this study to get evidence to confirm whether which approach is more appropriate and more successful in such fractures. Moreover, the findings of this research could profoundly influence clinical outcomes by guiding orthopedic surgeons in their decision-making for management of humeral midshaft fracture.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Presenting with humeral midshaft fracture (presence of fracture in the middle part or center of humerus )

Disqualifiers

Patients with pathological or open fractures, concomitant fractures or ligament or tendon ruptures of elbow or shoulder joints (on clinical examination)

Patients presented after 14 days of injury, partial or complete disability of the elbow or shoulder joint on the affected side before injury

Previous surgical procedure on same side

Presence of neurovascular complications

Trial design

Design model

Parallel

Treatments tested in this trial

  • Open Reduction Internal Fixation (ORIF) using Anterior approach for plate fixation

    Procedure/Surgery

    In group A, participants will undergo ORIF by using anterior approach for plate fixation. Operative time will be noted. After surgery, patients will be shifted to post-surgical orthopedic wards and will be discharged from there. All patients will be followed-up in OPD for 3 months.

  • Open Reduction Internal Fixation (ORIF) using Posterior approach for plate fixation

    Procedure/Surgery

    In group B, participants will undergo ORIF by using posterior approach for plate fixation. Operative time will be noted. After surgery, patients will be shifted to post-surgical orthopedic wards and will be discharged from there. All patients will be followed-up in OPD for 3 months.

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: Group A participantsExperimental treatment 1 intervention
Group B: Group B participantsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Operative time

It will be assessed by using in terms of minutes required to perform surgery from time of incision given in the skin until closure of skin with stitches.

Time frame
3 Months
2

Bone union

It will be labeled if there is detectable callus bridge or at least three visible cortices on radiographs

Time frame
3 Months
3

American Shoulder and Elbow Surgeons Score (ASES)

It will be assessed after 3 months of surgery

Time frame
3 Months

Secondary outcomes

Other outcomes

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

Sahiwal Teaching HospitalRecruiting57450, Sāhīwāl, Punjab ProvincePakistanPakistan

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Dr Jahanzaib Ramay

Lead sponsor

Sahiwal Teaching Hospital

Sponsor institution

Sahiwal Teaching Hospital

Collaborator