Vitagel Revision Total Knee Arthroplasty

A Prospective Randomized Evaluation of a Collagen/Thrombin Autologous Platelet Hemostatic Agent During Revision Knee Arthroplasty

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.

Study Overview

• Status: Terminated
• Conditions: Failed Total Knee Arthroplasty
• Intervention / Treatment: Device: Vitagel

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.

• Study Type: Interventional
• Enrollment (Actual): 8
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Ohio
    • Cleveland, Ohio, United States, 44195
      • The Cleveland Clinic

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 85 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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:

• The following exclusion criteria address safety and follow-up concerns or contraindications that could confound the study. If a patient exhibits any one of the following criteria, the patient is not eligible to participate in this study:

  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.

Exclusion Criteria (Intra-operative)

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Treatment Group; Vitagel	Device: Vitagel; Vitagel
No Intervention: Control; Standard of care for surgical hemostasis.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Transfusion Requirements	The primary objective of this study is to test for significant differences in transfusion requirements in patients managed with RTKA.	Participants will be followed for the duration of hospital stay, an expected average of 12 weeks.

Collaborators and Investigators

• Sponsor: The Cleveland Clinic
• Collaborators: Stryker Nordic
• Investigators: Principal Investigator: Trevor Murray, MD, The Cleveland Clinic

Study record dates

Study Major Dates

• Study Start: April 1, 2013
• Primary Completion (Actual): March 1, 2014
• Study Completion (Actual): March 1, 2014

Study Registration Dates

• First Submitted: July 26, 2013
• First Submitted That Met QC Criteria: August 14, 2013
• First Posted (Estimate): August 16, 2013

Study Record Updates

• Last Update Posted (Actual): June 7, 2017
• Last Update Submitted That Met QC Criteria: May 5, 2017
• Last Verified: May 1, 2017

More Information

Terms related to this study

• Other Study ID Numbers: 12-1128

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No
• IPD Plan Description: Study terminated early