Vitagel Revision Total Knee Arthroplasty

NCT ID: NCT01923805

Last Updated: 2017-06-07

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 8 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-04-30
• Study Completion Date: 2014-03-31

Brief Summary

This prospective study will evaluate the effectiveness of Vitagel (VG) in reducing blood loss associated with Revision Total Knee Arthroplasty (RTKA) procedures by assessing the patient's change in hemoglobin/hematocrit. Transfusion rates with the use of VG compared to the current standard of care will also be evaluated. The effectiveness of VG to potentially reduce pain, and increase return to function and quality of life will be assessed through the modified Knee Injury and Osteoarthritis Outcome Score (Modified KOOS), the Numerical Assessment Pain Scale (NAPS), and the SF-12 health survey. Analgesic use will be recorded post-operatively.

Detailed Description

This is a prospective, randomized, blinded clinical trial involving 4 orthopedic surgeons who perform Revision Total Knee Arthroplasty (RTKA), including Trevor Murray (PI), Viktor Krebs, Robert Molloy, and Carlos Higuera. A total of eighty subjects scheduled for RTKA, who meet all inclusion criteria and exhibit none of the exclusion criteria will be invited to participate in the study. Only subjects who sign the Institutional Review Board-approved Informed Consent Form will be entered into the Study.

In the forty treatment Subjects, VG will be applied to each surgical site. The forty control subjects will receive the surgeon's standard of care, without the use of any other hemostatic agents. The subjects will not be informed of their assignment, and the research investigator making the determination on blood transfusion requirements for all study subjects will also be blinded to the subject assigned arm of the study. The research investigator performing RTKA will remain blinded to the study arm until the randomization envelope is opened, which will take place during surgery, after hemostasis is achieved using bovie electrocautery, and prior to closure of the knee capsule.

Assessments will be made per the Time and Events Schedule.

Subjects will be evaluated for intra- and post-operative complications, and all such events, should they occur, will be recorded during the course of the study. Details describing the event, cause of event, its treatment and resolution will be documented.

Conditions

Failed Total Knee Arthroplasty

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Treatment Group

Vitagel

Group Type: EXPERIMENTAL

Vitagel

Intervention Type: DEVICE

Vitagel

Control

Standard of care for surgical hemostasis.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Vitagel

Vitagel

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Patients must meet all of the following criteria in order to be considered appropriate candidates for participation in the study:

1. Is scheduled for RTKA (may be the second stage/reimplantation of a two-stage revision for infection);

2. Is able and willing to provide voluntary written informed consent for participation in the study and able to comply with protocol requirements;

3. Is between the ages of 18 and 85 at the time of surgery. Both male and female will be included;

4. Is physically and mentally willing and able to comply with the clinical and evaluation follow-up schedule;

Exclusion Criteria

1. Is known to be sensitive to any materials of bovine origin;

2. Is undergoing a bilateral RTKA;

3. Is undergoing a single component revision (i.e. tibial or femoral component only)

4. Is undergoing a polyethylene revision only

5. Is predonating autologous blood;

6. Have a preoperative platelet count of less than 100,000

7. Have a previous history of venous thromboembolism or deep vein thrombosis;

8. Have a medical condition requiring anticoagulation

9. Currently using Coumadin;

10. Have a history of Heparin induced thrombocytopenia or Lovenox induced thrombocytopenia;

11. Have a history of rheumatoid arthritis or inflammatory arthritis;

12. Have peripheral vascular disease;

13. Have evidence of bleeding or metabolic-based hemolytic disorder (hemophilia or anticoagulation use), or hypercoaguable disorder;

14. Have a history of liver disease. Patients with liver dysfunction from cirrhosis or hepatitis may have impaired production of factors in the clotting cascade which may make these individuals more prone to bleed, especially with the use of anticoagulants. For this reason, these patients will also be excluded from the study if a baseline INR is greater than 1.3 or APTT greater than 32.4;

15. Have a history of failed treatment for abuse of, or are actively abusing, illegal drugs, solvents, or alcohol;

16. Have a systemic infection or infection at site of surgery;

17. Is a prisoner;

18. Is pregnant or nursing and;

19. Have a condition deemed by physician or medical staff to be non-conducive to patient's ability to complete the study, or a potential risk to the patient's health and well-being.

1. Clinical evidence of cancer and/or infection at surgical site

2. Use during the procedure of any other approved or unapproved product for the purpose of hemostasis

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Stryker Nordic

INDUSTRY

Sponsor Role: collaborator

The Cleveland Clinic

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Trevor Murray, MD

Role: PRINCIPAL_INVESTIGATOR

The Cleveland Clinic

Locations

The Cleveland Clinic

Cleveland, Ohio, United States

Countries

United States

Other Identifiers

12-1128

Identifier Type: -

Identifier Source: org_study_id