Clinical Trial Details
— Status: Recruiting
Administrative data
NCT number |
NCT05315284 |
Other study ID # |
Soh-Med-22-02-08 |
Secondary ID |
|
Status |
Recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
December 1, 2021 |
Est. completion date |
December 1, 2022 |
Study information
Verified date |
March 2022 |
Source |
Sohag University |
Contact |
Mostafa Salah, Bachelor of Medicine, Bachelor |
Phone |
01002397597 |
Email |
doc.mostafasala7[@]gmail.com |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
The Clinical and Radiological Outcomes of the Use of Titanium Elastic Nail in The Fixation of
Fresh Non-comminuted Fracture Mid-shaft Clavicle
Description:
Introduction:
The midshaft clavicle fractures account for 3 to 5% of all injuries and 70 to 80% of all
clavicle fractures.[1,2] In young adults, these fractures are usually related to sports or
vehicle accidents, whereas in children and elderly, they are usually related to falls.[1,2]
In general, clavicle fractures are treated conservatively and have a good outcome. In 1960,
Neer reported a non-union rate of 0.1% with conservative treatment[3] and Rowe corroborated
these findings in 1968 and showed a nonunion rate of 0.8% in conservatively managed
patients.[4] Since then, however, other authors have failed to demonstrate similar good
results with conservative treatment.[5,6] This may be due to the fact that the initial series
included children and adolescents and their enormous potential for bone healing may have
skewed the results, and that patient-based scoring systems were not used in the initial
series to record the outcome.[7] Hill et al. showed that displacement of more than 20 mm
resulted in 15% non-union and 18% of the patients had thoracic outlet syndrome following
union.[5] McKee et al. noted reduced patient satisfaction due to asymmetry and cosmesis
following malunion in patients with more than 20 mm shortening.[6] Hence, more recently,
there has been a trend toward surgical fixation.
Surgery has been indicated for completely displaced fractures, potential skin perforation,
shortening of clavicle by more than 20 mm, neurovascular injury, and floating injury.[8] The
gold standard for the surgical treatment has been open reduction and plate fixation through a
large incision.[8] Other surgical options include intramedullary pinning with Kirschner wire,
Rush pins, Knolwes pin, Steinman pin, Haige pin, ESIN (elastic stable intramedullary
nailing), and external fixation.[9] Intramedullary fixation for clavicular fractures was
first described by Peroni in 1950.[10] A systematic review showed relative risk reduction of
72% and 57% for non-union when using intramedullary fixation and plate fixation,
respectively, when compared with non-operative treatment of midshaft clavicle fractures.[11]
Intramedullary devices behave as internal splints that maintain alignment without rigid
fixation. The use of an intramedullary device carries advantages of a smaller incision, less
soft tissue dissection, load sharing fixation with relative stability that encourages copious
callus formation.[12] The titanium ESIN has been successfully used in fixation of pediatric
long bone fractures. One advantage of the titanium ESIN is that it can block itself in the
bone and provide a three-point fixation within the Sshaped clavicle.[8,13] However, some
studies have shown a relatively high complication rate and technical difficulties with
intramedullary nailing.[7,8] The aim of this study was to investigate the union rate and
complication rate of our patients with displaced midshaft clavicle fractures treated with
titanium ESIN. Aim of the study Investigating the union rate and complications rate following
titanium elastic stable intramedullary nailing (ESIN) for midshaft non-comminuted clavicle
fractures with >20 mm shortening/displacement. Materials and methods Place of the study:
Orthopaedics and Traumatology Department, Sohag University Hospital. Type of the study:
Prospective study. Study period: from December,2021 till December,2022. Inclusion criteria:
(1) Type IIA2 (angulation > 45 ) or IIB1 (shortening or overlapping displacement length > 2
cm) fresh unilateral midshaft clavicular fractures according to Robinson classification. (2)
Patient without underlying diseases such as primary hypertension and cardiac diseases.
Exclusion criteria: (1) pathological fractures. (2) multiple injuries of upper limbs. (3)
open fractures. (4) combined with injuries of blood vessels or nerves. (5) other diseases
which affected the functions of upper limbs. (6) Proximal and distal clavicular fractures.
(7) Comminuted clavicular fractures. Preoperative assessment: (1) Clinical evaluation: pain,
tenderness, deformity, shortening, skin tethering and loss of function. (2) Radiological
assessment: plain X-ray imaging is the corner stone for establishing the diagnoses of
clavicular fractures. CT scans can be used to exclude comminuted clavicular fractures if the
comminution of the fracture couldn't be visualized by the plain X-ray studies (3) Laboratory
assessment: routine laboratory investigations for any surgery.
Standard protocol approvals and patient consents:
This study will be approved by the Medical Research Ethics committee at faculty of medicine,
Sohag University. An informed written consent will be obtained from each patient.
Surgical technique:
After administration of anesthesia, the patient is placed in beach chair position with
injured extremity prepared and draped from the midline to the upper arm. Care is taken to
make sure that the sternoclavicular joint was accessible for the entry point. Preoperatively,
the shoulder region is screened using image intensifier to confirm this access. A vertical
skin incision is made just lateral to the sternoclavicular joint. The subcutaneous fat is
incised along with platysma. The pectoral fascia is divided in line with the skin incision
followed by careful elevation of the underlying musculature from the clavicle. The entry
point in the anterior cortex with a 3.2 mm drill bit and guide. The entry portal may be
enlarged with an awl and appropriate sized titanium ESIN is inserted (The size of the nail
was measured using this formula = 0.4 × canal diameter in mm). Attempt is made to close
reduce the fracture. If the fracture could not be reduced by closed means, then a separate
vertical incision is used at the fracture site to aid fracture reduction. Vertical incision
is used as it is parallel to Langer's lines and minimizes the risk of damage to
supraclavicular nerves to avoid dysesthesia of skin and scar neuromas. The nail is used to
create a path in the lateral end of the clavicle for subsequent easy access.
The nail is then passed from the medial side and across the reduced fracture into the lateral
end of clavicle.
Postoperative management:
All patients are treated with arm sling after operation for 6 weeks. In addition, 3 days
after surgery, patients are allowed to do passive anteflexion and abduction motion of
shoulder joint under the guidance of physiotherapists, and the motion range could be
increased gradually depending on the degree of pain. However, the range of passive
anteflexion and abduction motion is kept within 90 degrees in 6 weeks after surgery, and the
weight-bearing exercise is not allowed. The range of passive and active motion is increased
gradually according to the condition of fracture union and the weight-bearing exercise is
started gradually after 6 weeks post-operatively. The postoperative follow-up visits are
scheduled every two weeks until bone union and every 3 months after bone union.
Post-Operative Evaluation
Evaluation of therapeutic efficiency:
The operative data is recorded and analyzed, including operation time, blood loss, hospital
stays and postoperative complications. The standards of bone union includes the formation of
continuous callus and the disappearance of fracture line, no tenderness of the fracture ends,
and no subjective pain when performing active sports and weight-bearing activities on the
clinical examinations.
Scoring system:
Improvement of subjective pain is assessed using a visual analog scale (VAS) at 1 day before
surgery and 3 days after surgery. The flexion and abduction motion ranges of shoulder joint
were recorded from one day before surgery to the last follow-up.24 Shoulder function is
assessed with the Constant-Murley score (range: 0-100 points, best: 100) and the Disabilities
of the Arm, Shoulder and Hand (DASH) score (range: 0- 100 points, best: 0) at the last
follow-up. In detail, Constant-Murley scores are categorized as follows: excellent (90-100),
good (80-89), satisfactory (70-79), and fair (<70). DASH scores of 0-10 are considered as an
excellent result, and score >40 is associated with poor shoulder function.