Current partner codePEPTIDESDE
NCT01896011·Phase 3·INTERVENTIONAL

Effect of Teriparatide on Fracture Healing in Patients With Incomplete Atypical Femur Fractures

Status

Completed

Phase

Phase 3

Enrollment

34

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

Atypical femur (thigh bone) fractures (AFFs) are uncommon low-trauma fractures which often occur without warning, are highly debilitating, and are slow to heal. As physicians learn more about them, AFFs are increasingly being identified prior to a total break. However, there's no evidence on the best way to treat these non-displaced AFFs. One option is teriparatide, an osteoporosis medication that can build new bone. Investigators will conduct a double blind randomized placebo controlled trial to examine whether teriparatide use in AFF patients with an incomplete break will help accelerate fracture healing and prevent surgical intervention. Co-primary outcomes include change in WOMAC scores from baseline to 12 months and number of participants requiring surgical intervention at 12 months. Investigators will recruit 60 women and men over the age of 30 who have experienced an incomplete AFF. Participants will be randomly assigned to either teriparatide (20 mcg/day) or placebo (using an identical injection pen) for up to 2 years. As AFFs are highly debilitating, a trial examining the use of Teriparatide in this population is urgently needed.

Interventions

Treatment arms and agents.

BIOLOGICAL

Teriparatide 20 mcg

Teriparatide 20 mcg injection pen

OTHER

Placebo

Placebo 20 mcg injection pen

Timeline

From registration to results.

  1. First posted

    Jul 11, 2013

  2. Study start

    Jul 2013

  3. Primary completion

    Dec 2021

  4. Study completion

    Dec 2022

  5. Results posted

    Not reported

  6. Registry updated

    Jun 1, 2023

Outcomes

What the study measures.

Primary outcomes

Change in the modified The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)of the affected limb (the femur that has the incomplete AFF)

Time frame · baseline to 12 months

The proportion of patients requiring surgical intervention

Time frame · baseline to 12 months

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
30 Years
Maximum age
100 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: i. Female or male; ii. Over the age of 30; iii. Experienced an incomplete AFF that satisfies the diagnostic criteria as set forth by the American Society for Bone and Mineral Research (ASBMR) International Task Force on AFFs: 1. Atraumatic or low trauma incomplete stress fractures, defined as fractures sustained with minimal force, such as a fall from standing height; 2. From distal to the lesser trochanter to proximal to the supracondylar flare along the femoral shaft. 3. Radiographic confirmation of AFF features is required for a definitive diagnosis. Incomplete AFF features include cortical thickening, cortical beaking, and lucency line. Patients with cortical beaking without lucency line can be included. Exclusion Criteria: i. Peri-prosthetic fractures, ii. High trauma fractures, iii. Pathological fractures secondary to metastases or metabolic bone diseases other than osteoporosis, iv. Fractures that are not confirmed by radiological investigations, v. Contraindication to use of teriparatide such as: 1. pregnant or nursing mothers, or women who are planning on pregnancy within 1 year of completing teriparatide therapy, 2. hypersensitivity to teriparatide, 3. severe renal impairment, 4. multiple myeloma, 5. active cancer in past 5 years (other than non-melanoma skin cancer), 6. primary hyperparathyroidism, 7. hypercalcemia, 8. Paget's disease or other conditions that may increase the risk for osteosarcoma, 9. Prior radiation therapy involving the skeleton, vi. Concomitant use of other osteoporosis therapies including bisphosphonates or denosumab (except calcitonin). AFF patients with complete fractures on the contralateral side or patients with secondary osteoporosis will not be excluded.

Study locations

1 registered sites.

Canada. Showing up to 24 locations stored in the fast local snapshot.

University Health Network

Toronto, Ontario, Canada

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Teriparatide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.