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Extended Postoperative Oral Tranexamic Acid in Knee Replacement

Primary Purpose

Knee Osteoarthritis, Blood Loss, Pain, Postoperative

Status
Active
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Tranexamic Acid Pill
Placebo
Sponsored by
Campbell Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Knee Osteoarthritis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Primary total knee replacement in ambulatory setting
  • Willing to participate
  • Physical therapy on site at Campbell Clinic Wolf River
  • Fluent in oral and written English

Exclusion Criteria:

  • Unwilling to participate
  • Revision total knee replacement
  • Preoperative use of anticoagulants other than 81 mg aspirin
  • Previous history of thromboembolic event
  • Previous history of cancer other than non-melanoma skin cancers

Sites / Locations

  • Campbell Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Oral TXA

Oral placebo

Arm Description

1,950 mg oral tranexmic acid (three capsules of 650 mg) administered in post-anesthesia care, postop day one and postop day two. Compounded by registered pharmacist and labeled with subject name and instructions for use.

Three capsules of cellulose administered in post-anesthesia care, postop day one and postop day two. Compounded by registered pharmacist and labeled with subject name and instructions for use.

Outcomes

Primary Outcome Measures

Hemoglobin level
Hemoglobin enables red cells to transport oxygen and carbon dioxide in the blood and is measured in grams per deciliter with normal ranges of 12.0 to 17.5
Hemoglobin level
Hemoglobin enables red cells to transport oxygen and carbon dioxide in the blood and is measured in grams per deciliter with normal ranges of 12.0 to 17.5
Hemoglobin level
Hemoglobin enables red cells to transport oxygen and carbon dioxide in the blood and is measured in grams per deciliter with normal ranges of 12.0 to 17.5
Hemoglobin level
Hemoglobin enables red cells to transport oxygen and carbon dioxide in the blood and is measured in grams per deciliter with normal ranges of 12.0 to 17.5

Secondary Outcome Measures

Visual Analog Score
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Visual Analog Score
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Visual Analog Score
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Visual Analog Score
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Visual Analog Score
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
KOOS Jr Score
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
KOOS Jr Score
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
KOOS Jr Score
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
KOOS Jr Score
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
KOOS Jr Score
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
KOOS Jr Score
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
range of motion of knee
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
range of motion of knee
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
range of motion of knee
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
range of motion of knee
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
range of motion of knee
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion

Full Information

First Posted
October 11, 2021
Last Updated
August 25, 2023
Sponsor
Campbell Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT05099276
Brief Title
Extended Postoperative Oral Tranexamic Acid in Knee Replacement
Official Title
Extended Postoperative Tranexamic Acid Use in Primary Total Knee Arthroplasty: A Prospective, Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 7, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
June 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Campbell Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A comparison of outcomes between use of oral tranexamic acid as compared to oral placebo in the first days after total knee replacement will be made to determine impact on clinical indications and patient reported outcomes.
Detailed Description
Significant blood loss occurs during total knee arthroplasty (TKA) which can lead to adverse outcomes including need for blood transfusion as well as increased local tissue swelling and ecchymosis which can inhibit post-operative recovery. Tranexamic acid (TXA), an inhibitor of fibrinolysis, has been shown to be a safe and effective drug for reducing blood loss during and after TKA. The use of TXA intraoperatively has been associated with higher postoperative hemoglobin levels and a reduction in postoperative blood transfusion rates. Administration of TXA in TKA has also been associated with improved clinical outcome measures including decreased rate of periprosthetic joint infection, decreased length of stay, and increased postoperative range of motion and early ambulation distances. However, there remains a wide variance in the route of administration, dosage, and timing of TXA use among treatment protocols in TKA. Previous studies have evaluated outcomes with the addition of post-operative TXA dosing to standard pre-operative and intra-operative intravenous (IV) doses. This study will investigate patient outcomes following a standardized post-operative oral TXA protocol as compared to oral placebo for three doses over day of surgery, postop day one and postop day two after TKA. Following written consent documentation, Subjects will be randomized and blinded to randomization assignment until completion of study to either the oral TXA group or oral placebo group. The study medication will be distributed with the Subject's name with instructions for use in the post-anesthesia unit (PACU). The first dose will be administered in PACU with subsequent doses to be taken at home on postop day one and postop day two. TKA will be completed in an ambulatory surgery center with discharge same day of surgery to home. Outcome measures include: Hemoglobin, visual analog score, KOOS Jr (Knee injury and osteoarthritis outcome score), range of motion, and incidence of treatment-emergent adverse event at postoperative (POD) day 3, POD week 2, POD week 6, and POD week 12. KOOS Jr. will be collected at one year post-op.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis, Blood Loss, Pain, Postoperative

7. Study Design

Primary Purpose
Other
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
Both oral TXA and oral placebo will be distributed to subjects in bottle marked with subject name and instructions for use following discharge from PACU.
Allocation
Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Oral TXA
Arm Type
Experimental
Arm Description
1,950 mg oral tranexmic acid (three capsules of 650 mg) administered in post-anesthesia care, postop day one and postop day two. Compounded by registered pharmacist and labeled with subject name and instructions for use.
Arm Title
Oral placebo
Arm Type
Placebo Comparator
Arm Description
Three capsules of cellulose administered in post-anesthesia care, postop day one and postop day two. Compounded by registered pharmacist and labeled with subject name and instructions for use.
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid Pill
Intervention Description
1950 mg tranexamic acid (three capsules) given in post-anesthesia room and three capsules for postop day one and three capsules for postop day two
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Three capsules of cellulose given in post-anesthesia room and three capsules for postop cay one and three capsules for postop day two
Primary Outcome Measure Information:
Title
Hemoglobin level
Description
Hemoglobin enables red cells to transport oxygen and carbon dioxide in the blood and is measured in grams per deciliter with normal ranges of 12.0 to 17.5
Time Frame
preoperative
Title
Hemoglobin level
Description
Hemoglobin enables red cells to transport oxygen and carbon dioxide in the blood and is measured in grams per deciliter with normal ranges of 12.0 to 17.5
Time Frame
postoperative hour 3
Title
Hemoglobin level
Description
Hemoglobin enables red cells to transport oxygen and carbon dioxide in the blood and is measured in grams per deciliter with normal ranges of 12.0 to 17.5
Time Frame
postoperative day 3
Title
Hemoglobin level
Description
Hemoglobin enables red cells to transport oxygen and carbon dioxide in the blood and is measured in grams per deciliter with normal ranges of 12.0 to 17.5
Time Frame
postoperative week 2
Secondary Outcome Measure Information:
Title
Visual Analog Score
Description
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Time Frame
preoperative
Title
Visual Analog Score
Description
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Time Frame
postoperative hour 3
Title
Visual Analog Score
Description
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Time Frame
postoperative week 2
Title
Visual Analog Score
Description
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Time Frame
postoperative week 6
Title
Visual Analog Score
Description
Patient reported pain score from 0 to 10 where 0 is no pain and 10 is the most pain
Time Frame
postoperative week 12
Title
KOOS Jr Score
Description
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
Time Frame
preoperative
Title
KOOS Jr Score
Description
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
Time Frame
postoperative day 3
Title
KOOS Jr Score
Description
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
Time Frame
postoperative week 2
Title
KOOS Jr Score
Description
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
Time Frame
postoperative week 6
Title
KOOS Jr Score
Description
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
Time Frame
postoperative week 12
Title
KOOS Jr Score
Description
Patient reported outcome of how the knee feels from 0 to one 100 where 0 represents extreme problems and 100 represents no problems
Time Frame
postoperative one year
Title
range of motion of knee
Description
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
Time Frame
preoperative
Title
range of motion of knee
Description
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
Time Frame
postoperative day 3
Title
range of motion of knee
Description
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
Time Frame
postoperative week 2
Title
range of motion of knee
Description
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
Time Frame
postoperative week 6
Title
range of motion of knee
Description
clinical measurement of passive, pain-free range of motion of knee in degrees from 0 to 180 from maximum extension to maximum flexion
Time Frame
postoperative week 12
Other Pre-specified Outcome Measures:
Title
Incidence of treatment-emergent adverse event
Description
monitoring for safety events
Time Frame
postoperative day 3
Title
Incidence of treatment-emergent adverse event
Description
monitoring for safety events
Time Frame
postoperative week 2
Title
Incidence of treatment-emergent adverse event
Description
monitoring for safety events
Time Frame
postoperative week 6
Title
Incidence of treatment-emergent adverse event
Description
monitoring for safety events
Time Frame
postoperative week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Primary total knee replacement in ambulatory setting Willing to participate Physical therapy on site at Campbell Clinic Wolf River Fluent in oral and written English Exclusion Criteria: Unwilling to participate Revision total knee replacement Preoperative use of anticoagulants other than 81 mg aspirin Previous history of thromboembolic event Previous history of cancer other than non-melanoma skin cancers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcus C Ford, MD
Organizational Affiliation
Campbell Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Campbell Clinic
City
Germantown
State/Province
Tennessee
ZIP/Postal Code
38138
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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29699826
Citation
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Results Reference
background
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28870300
Citation
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Citation
Prasad N, Padmanabhan V, Mullaji A. Blood loss in total knee arthroplasty: an analysis of risk factors. Int Orthop. 2007 Feb;31(1):39-44. doi: 10.1007/s00264-006-0096-9. Epub 2006 Mar 28.
Results Reference
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Citation
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Citation
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Citation
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Citation
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Extended Postoperative Oral Tranexamic Acid in Knee Replacement

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