Trial Search Results

Safety and Efficacy Study of Treatment of Pathological Fractures in Humerus

This study will collect safety and performance data of the Photodynamic Bone Stabilization System (PBSS) when used for the treatment of fractures of the humerus secondary to metastatic cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

IlluminOss Medical, Inc.

Stanford Investigator(s):

Intervention(s):

  • Device: Photodynamic Bone Stabilization System

Phase:

N/A

Eligibility


Inclusion Criteria:

- General Inclusion Criteria

   1. Skeletally mature adult males and females 18 years of age or older.

   2. Impending or actual pathological fracture of the humerus, secondary to metastatic bone
   disease.

   3. Females: neither pregnant nor intending to become pregnant during the course of the
   study, defined as:

      1. Postmenopausal for at least 1 year OR

      2. Documented oophorectomy or hysterectomy

      3. Surgically sterile OR

      4. If of childbearing potential, must be practicing double-barrier method of birth
      control, be willing to avoid pregnancy for the period of study participation and
      have a negative pregnancy test at screening

   4. Patient, or his/her legally authorized representative, is able to understand and
   provide informed consent.

   5. Willing and able to comply with post-operative treatment protocol and follow-up visit
   schedule.

   6. VAS Pain Score > 60mm on 100mm scale.

   -Impending Fracture-Specific Inclusion Criteria

   7. Documented presence of at least one metastatic lesion of the humerus.

   8. Mirels Criteria Score ≥ 8. (specific to the target humeral lesion and subject to
   minimum VAS score requirements)

   9. Destruction of cortical bone at impending fracture site > 50%.

   -Actual Fracture-Specific Inclusion Criteria

10. Fracture is closed, Gustilo Type I or II.

Exclusion Criteria:

- General Exclusion Criteria

   1. Primary tumor (osteogenic origin, etc.) at site.

   2. Impending or actual fracture at any other location that, in the Investigator's
   opinion, would preclude ability to assess pain and/or function in the target humerus.

   3. Active or incompletely treated infections that could involve the device implant site.

   4. Distant foci of infection that may spread to the implant site.

   5. Allergy to implant materials or dental glue.

   6. In the investigator's judgment, functional deficit in the target humerus with an
   etiology other than bone metastases (e.g. due to vascular insufficiency).

   7. In the investigator's judgment, focal neurologic deficit as a result of metastases in
   the brain, spine, or other central nervous system disorders.

   8. Uncooperative patients, or patients who are incapable of following directions (for
   example, as a consequence of a neurological or psychiatric disorder).

   9. Prisoner

   -Impending Fracture-Specific Exclusion Criteria

10. Mirels Score < 8 (specific to target humeral lesion).

11. Destruction of cortical bone at impending fracture site < 50%.

12. Prior surgery and/or prior fracture of affected site.

13. Any articular component to impending fracture site.

   -Actual Fracture-Specific Exclusion Criteria

14. Open fractures with severe contamination.

15. Extremely comminuted fractures where insufficient holding power of the balloon on the
   intramedullary canal is probable.

16. Patients whose intramedullary canal at site of fracture measures smaller than the
   diameter of the sheath provided.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cancer Clinical Trials Office
650-498-7061
Not Recruiting