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Percutaneous Intramedullary K-wires Fixation of Pediatric Shaft Both Bone Forearm Fractures

Percutaneous Intramedullary K-wires Fixation of Pediatric Shaft Both Bone Forearm Fractures

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05744349
Enrollment
20
Registered
2023-02-27
Start date
2023-02-28
Completion date
2024-04-01
Last updated
2023-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fracture Fixation, Intramedullary, Fracture Forearm

Brief summary

This study is to improving outcome of pediatric both bone forearm fractures using minimally invasive procedure by intramedullary K-wires.

Detailed description

Most shaft injuries present no unusual challenges and require nothing more than skillful closed reduction and cast immobilization due to the unique property of the growth potential of the immature skeleton. There is a relatively high incidence of re-displacement, malunion and consequent limitation of movement. Perfect anatomical reduction is not always necessary since remodeling of malunion may correct any residual deformity. Angulation has been shown to affect the range of pronation and supination of the forearm. The most common indications for surgery are failure of closed reduction, open fractures, and fracture instability. When operative intervention is indicated different techniques can be employed such as intramedullary nailing, osteosynthesis with plate and screws fixation and external fixators. Intramedullary nailing has been shown to produce excellent clinical results and in contrast to plate fixation is considered as a minimal invasive procedure. Surgical technique of K-wires : After administration of anesthesia, surgery will be performed with the patient supine on the operating table and fracture will be analyzed with an image intensifier. In radius, the wire will be inserted by surgical drilling through Lister's tubercle or the radial styloid while in ulna, the wire will be inserted through the tip of the olecranon.

Interventions

PROCEDUREK-wires Fixation of Pediatric Shaft Both Bone Forearm Fractures

After administration of anesthesia, surgery will be performed with the patient supine on the operating table and fracture will be analyzed with an image intensifier. In radius, the wire will be inserted by surgical drilling through Lister's tubercle or the radial styloid while in ulna, the wire will be inserted through the tip of the olecranon.

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

After administration of anesthesia, surgery will be performed with the patient supine on the operating table and fracture will be analyzed with an image intensifier. In radius, the wire will be inserted by surgical drilling through Lister's tubercle or the radial styloid while in ulna, the wire will be inserted through the tip of the olecranon.

Eligibility

Sex/Gender
ALL
Age
4 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who are younger than the age of 10 years old from both genders and suffering from displaced fractures of shaft both bone of the forearm; 2. Standard preoperative anteroposterior (AP) and lateral forearm radiographs; 3. Complete clinical and radiographic data.

Exclusion criteria

1. Poly-traumatized patients with other associated fractures; 2. Undisplaced fractures; 3. Open fractures; 4. Pathological fractures; 5. Malignancy; 6. Malnutrition; 7. Chronic diseases as renal, hepatic, cardiac patients; 8. Incomplete radiographic data.

Design outcomes

Primary

MeasureTime frame
Union of fractures1 month
Degree of flexion and extension at wrist joint3 months
Degree of supination and pronation3 months

Countries

Egypt

Contacts

Primary ContactMahmoud H Abdelmajeed, Resident
Mahmood-h-2010@outlook.com01201605995
Backup ContactAhmad I Addosooki, Professor
01011110232

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026