Supracondylar Distal Femur Fractures and Abaloparatide

Daniel Horwitz

Status and phase: Withdrawn; Phase 4

Conditions: Femoral Fractures

Treatments: Drug: Abaloparatide; Drug: Placebo

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04626141

2020-0544

Details and patient eligibility

About

Supracondylar femur fractures in the geriatric population present a unique challenge to the orthopaedic surgeon both in terms of fixation, healing, and final extremity axial alignment. Pulsed dosing of parathyroid hormone derivatives (Forteo) has been shown to increase bone mass, and several studies in Europe have demonstrated its benefit as an adjuvant for fracture healing. Abaloparatide represents a new compound which similarly offers great potential for accelerating fracture healing, especially healing associated with callous formation. This is a randomized, double blind placebo-controlled trial to compare a group of patients being treated for supracondylar distal femur fractures who receive abaloparatide (n=38) with a control group of patients who receive a placebo (n=38).

Full description

Supracondylar femur fractures in the geriatric population present a unique challenge to the orthopaedic surgeon both in terms of fixation, healing, and final extremity axial alignment. Multiple methods of fixation are well accepted, and each has its own advantages and disadvantages. The common occurrence of periprosthetic supracondylar femur fractures adds another level of complexity, and the universal goal when treating these patients is to obtain and maintain acceptable alignment, allow mobilization and early weight bearing, and achieve union. To a degree, mobilization and weight bearing compete with maintenance of axial alignment, and any final outcome is a race between healing and loss of fixation. As a result, any intervention that can accelerate healing would be of great benefit. As the vast majority of these injuries heal with secondary bone healing (callous), the determination of "healing" is reliably determined using the modified Radiographic Union Score for Tibia Fractures (mRUST), and thus this patient population offers an ideal population in which to evaluate an accelerant of fracture healing.

Pulsed dosing of parathyroid hormone derivatives (Forteo) has been shown to increase bone mass, and several studies in Europe have demonstrated its benefit as an adjuvant for fracture healing. Abaloparatide represents a new compound which similarly offers great potential for accelerating fracture healing, especially healing associated with callous formation. This is a randomized, double blind placebo-controlled trial to compare a group of patients being treated for supracondylar distal femur fractures who receive abaloparatide (n=38) with a control group of patients who receive a placebo (n=38).

Sex: All

Ages: 65+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Subject is ≥ 65 years old
2. Subject is willing and able to read, comprehend, and sign the study informed consent form in English prior to study specific procedure
3. Subject is being treated for a closed supracondylar distal femur fracture with either a retrograde nail or locked plate
4. Subject undergoes open reduction/fixation

Exclusion criteria

1. Subject has open fracture
2. Bilateral injury or other lower extremity injury that would affect weight bearing status
3. Subject's postoperative radiographs (on day of surgery) indicate failure to achieve axial alignment (more than 10 degrees axial alignment and more than 25% anterior/posterior displacement in lateral view)
4. Subject has additional severe traumatic conditions such as closed head injury
5. Subject has medical condition or is on medication that may significantly affect healing (i.e. immunosuppressive diseases and drugs)
6. Subject has active or history of Paget's disease of the bone, bone cancer, or other bone diseases or conditions placing them at increased risk of osteosarcoma
7. Subject has active or history of hypercalcemia or underlying hypercalcemic disorder, such as primary hyperparathyroidism
8. Subject has active or a history of urolithiasis
9. Subject will have trouble injecting the pen and does not have someone to help them on a daily basis

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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0 participants in 2 patient groups, including a placebo group

Abaloparatide group

Experimental group

Description:

Patients in the experimental group will receive abaloparatide after their surgery.

Treatment:

Drug: Abaloparatide

Control group

Placebo Comparator group

Description:

Patients in the control group will receive a placebo after their surgery.

Treatment:

Drug: Placebo