Burst Biologics Foot and Ankle Registry

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT03077256

FA002

Ages > 18
All Genders

Study Summary

This prospective registry was designed as an observational study to ascertain how commercially available Burst Products are being used by foot and ankle surgeons performing procedures which involve bone grafting, as well as determining relevant patient outcomes.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Patient aged 18 years or older
Patient diagnosed with a pathology of the hindfoot, foot, or ankle requiring surgicalintervention.
The surgeon has determined that a Burst Biologic product is or was clinicallyindicated.
Patient capable of understanding the content of the Informed Consent Form.
Patient willing and able to participate in the registry protocol including thesurgeon's standard follow-up visits and clinical evaluations.
Patient who has agreed to participate in the registry by providing consent per theapplicable local law and the declaration of Helsinki.

Exclusion

Exclusion Criteria: The following are relative contraindications for the use of BurstProducts, however the investigator surgeon is solely responsible for the determination ofpatient eligibility for surgery:

Severe vascular or neurological disease
Uncontrolled diabetes
Severe degenerative disease (other than degenerative disc disease)
Hypercalcemia, abnormal calcium metabolism
Existing acute or chronic infections, especially at the site of the operation
Inflammatory bone disease such as osteomyelitis
Malignant tumors
Patients who are or plan to become pregnant.

Study Design

March 24, 2017

October 01, 2020

Study Description

Foot and ankle surgery requiring the use of bone graft is common despite recent advancements and improved outcomes with new motion preservation devices (ankle replacement). Autogenous bone remains the gold standard but is complicated by donor site morbidity and availability of a sufficient volume of graft. Over the past two decades surgeon interest in alternative bone grafts has steadily increased. Bone morphogenic proteins, synthetic bone graft substitutes, and various allograft products are widely available to surgeons. Limitations on the use of allografts in the past were mainly attributed to less than optimal donor screening and processing techniques which removed viable components needed to aid in the bone healing process.

In recent years, the focus and scientific advances in various allograft processing techniques have allowed the retention of various viable cytokines, growth factors, and cell populations which result in enhanced osteogenic and osteoinductive properties. Rigorous donor bone screening and meticulous testing has virtually eliminated the risk of disease transmission.

A unique proprietary cryoprotection processing technique for allograft tissue was developed by Smart-Surgical, Inc. and a complete line of allograft products was created and is now marketed by Burst Biologics (dba). In addition, rigorous standardized laboratory assay techniques and statistical analysis provide consistency and uniformity of the biologically active components of Burst allograft products.

Connect with a study center

Georgetown University Medical Center
Washington, District of Columbia 20007
United States
Active - Recruiting
Rocky Mountain Foot and Ankle
Caldwell, Idaho 83605
United States
Site Not Available

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