Peroneal and Achilles Tendon Repair Indications With CLARIX® CORD 1K (PATRICC)

A

Amniox Medical

Status

Completed

Conditions

Peroneal and Achilles Tendon Tears

Treatments

Other: CLARIX® CORD 1K graft

Study type

Interventional

Funder types

Industry

Identifiers

NCT02719288
CR-2010

Details and patient eligibility

About

Peroneal and Achilles tendon tears are common diseases that present challenges to surgeons due to tendon adhesion complications. Functional recovery is compromised by limiting post-operative range of motion, mobility, and can lead to considerable amount of post-operative pain for the patient. Amniotic membrane tissue has demonstrated clinical success as an anti-inflammatory and anti-scarring agent and promoting wound healing towards regeneration. Cryopreserved human amniotic membrane and umbilical cord (AM/UC) tissue in the form of CLARIX® CORD 1K has been used to treat over 5000 orthopedic patients. The investigators hypothesize that its use in peroneal and Achilles tendon surgical repair will enhance the overall functional recovery of the patient.

Enrollment

64 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Male and female patients 18 years to 80 years of age
  2. Confirmed tendon pathology via MRI, if clinically necessary, with planned surgical repair that have failed conservative management (PT) for a minimum of 2 months for chronic and partial thickness tears; acute full thickness tears or tendon rupture immediately eligible.
  3. Willing to follow the instructions and complete the visits required.

Exclusion criteria

  1. Psychologically unstable
  2. Acute infections that, in the opinion of the investigator, may complicate healing
  3. Currently receiving chemotherapy
  4. Systemic inflammatory arthritis or Rheumatoid arthritis
  5. Uncontrolled diabetes as measured by A1C>12
  6. Bleeding disorders
  7. Unable to provide informed consent
  8. Has received oral or parenteral corticosteroids or cytotoxic agents for seven consecutive days in the period of 30 days before surgery OR has received a local steroid injection within 7 days of surgery
  9. Immunocompromised patients
  10. Active malignancy other than non-melanoma skin cancer
  11. Untreated alcohol or substance abuse issues at the time of screening
  12. Pregnant women at the time of randomization
  13. Currently enrolled or participated in another investigational device, drug, or biological trial within 60 days of screening
  14. Allergy to amphotericin-B or Dulbecco's Modified Eagle Medium (DMEM).
  15. Will undergo significant concurrent procedures with the tendon procedures on the affected foot that, in the opinion of the Investigator, may complicate healing or alter the post-operative visit schedule

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

64 participants in 2 patient groups

CLARIX® CORD 1K
Experimental group
Description:
Applied in addition to standard of care tendon repair surgery.
Treatment:
Other: CLARIX® CORD 1K graft
Standard of care tendon repair surgery only
No Intervention group

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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