Short Versus Long Intramedullary Nails in the Treatment of Proximal Femur Metastasis.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20+
SponsorNational Taiwan University Hospital

About this trial

The goal of this interventional randomized controlled trial is to compare the clinical outcomes in treating extremities pathological fractures (fractures of limbs caused by metastatic tumors) or impending pathological fractures with short or long intramedullary nails. The main questions it aims to answer are:

1. What is the rate of developing new distant metastasis of the operated extremities? 2. Does treating extremities (impending) pathological fractures with long intramedullary nails have lower or similar reoperation rate than the short nails? 3. Are there any differences when comparing the surgical-related complication, functional outcomes and life quality assessment between treating extremities (impending) pathological fractures with long or short intramedullary nails.

Participants who meet surgical indication will be randomized into either the long or short intramedullary nail group after informed consent. The patient will receive bone fixation with the corresponding prosthesis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Femur (impending) pathological fracture that is suitable for intramedullary nail fixation as determined by the physician

Patient is willing to participate in this clinical trial and cooperate with follow-up

Disqualifiers

The patient has a more appropriate treatment alternative to single intramedullary nail fixation as determined by the multidisciplinary decision, such as,

The metastatic lesions involved the femur head

The metastatic lesions involved the pelvis

The metastatic lesions compromised the greater or lesser trochanter to a certain extent that arthroplasty was indicated

Trial design

Design model

Parallel

Treatments tested in this trial

  • Internal fixation with short intramedullary nails

    Device

    Intramedullary nailing is a method of internal fixation used to treat fractures. An intramedullary nail is a metal rod forced into the marrow canal of a bone to stabilize and align fractures. Participants in this group will be fixed with a shorter intramedullary nail (defined as defined as less than 2/3 of the patient's femur) for proximal femoral (impending) pathological fractures.

  • Internal fixation with long intramedullary nails

    Device

    Intramedullary nailing is a method of internal fixation used to treat fractures. An intramedullary nail is a metal rod forced into the marrow canal of a bone to stabilize and align fractures. Participants in this group will be fixed with a longer intramedullary nail (defined as greater than 2/3 of the patient's femur) for proximal femoral (impending) pathological fractures.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Short intramedullary nailsExperimental treatment 1 intervention
Group B: Long intramedullary nailsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Reoperation rate

Percentage of patients receiving revision surgery within 1 year after the intervention. The primary outcome should be compared using non-inferior tests. The non-inferior margin was pre-specified at 25.4%.

Time frame
Up to 1 year after the intervention

Secondary outcomes

1

Change from baseline in functional outcome on the Patient-Reported Outcomes Measurement Information System-29 scoring at 1,3,6,12 months after the intervention

The Patient-Reported Outcomes Measurement Information System (PROMIS) is a set of person-centered measures that evaluates physical, mental, and social health in adults and children. It's used to measure symptoms and other aspects of health status in a wide variety of chronic diseases. PROMIS-29 is a particular version of this system that covers multiple domains of health and function. It consists of 29 items in total, spanning seven domains: physical function, anxiety, depression, fatigue, sleep disturbance, ability to participate in social roles and activities, and pain interference. Each domain has four questions, with the exception of the pain interference domain, which has five. Each question is scored from 1-5, the higher score indicates better function or quality of life. The sum of the PROMIS results in the raw score, which lies between 4 and 20. There's also a single question evaluating pain intensity, as assessed by pain intensity numeric rating scale.

Time frame
At 1,3,6,12 months after the intervention
2

Cardiopulmonary complication rate within 30 days after the intervention

Cardiopulmonary complication includes the following events developing within 30 days after the intervention: O2 desaturation, shock, embolic event, or coma and death.

Time frame
Up to 30 days after the intervention
3

Mortality rate at 1,3,6,12 months after the intervention

Percentage of demise at 1,3,6,12 months after the intervention

Time frame
At 1,3,6,12 months after the intervention
4

Percentage of of participants with distant femoral metastasis

Newly formed metastatic lesions on the same limb distant to the operation site within 1 year after the intervention

Time frame
Up to 1 year after the intervention

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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

National Taiwan University Hospital

Lead sponsor

National Taiwan University Hospital, Yun-Lin Branch

Collaborator

National Taiwan University Hospital Hsin-Chu Branch

Collaborator

This trial is not recruiting at the moment. You can still explore other options: