Overview

Does Tranexamic Acid Improve Visualization During Arthroscopic Rotator Cuff Repair

Status:
Recruiting
Trial end date:
2022-04-01
Target enrollment:
0
Participant gender:
All
Summary
This clinical trial examines whether intravenous preoperative administration of tranexamic acid (TXA) before arthroscopic rotator cuff repair (ARCR) can improve arthroscopic visualization during the procedure.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Saskatchewan
Treatments:
Tranexamic Acid
Criteria
Inclusion Criteria:

- Age 18-100

- Male and Female

- Patient able to read and understand consent form

- Non-traumatic, simple small or medium sized rotator cuff tear as defined by
pre-operative MRI

- Booked to operating room for elective rotator cuff repair

- Beach chair positioning

Exclusion Criteria:

- Patient refusal to participate

- Massive rotator cuff tear

- Acute traumatic rotator cuff tear

- Known coagulopathy

- Patients with a history or risk of thromboembolism

- Known hypersensitivity to tranexamic acid

- Patient unable to be off anti-coagulant medication for long enough to counter effects

- Patient has a clinic systolic blood pressure > 150mmHg

- Lateral positioning

- Requirement or insistence by patient or anesthesiologist on regional block

- Patients who have smoked nicotine products within the last year

- The presence of other inflammatory conditions (calcific tendonitis, rheumatoid
arthritis, etc.)

- The presence of active thromboembolic disease, such as deep vein thrombosis, pulmonary
embolism, and cerebral thrombosis

- Patient has a seizure disorder

- Patients on medications identified as having drug-drug interactions (hormonal
contraceptive, hydrochlorothiazide, desmopressin, sulbactam-ampicilllin,
carbazochrome, ranitidine, or nitroglycerine

- Patient is pregnant

- Patients with history of subarachnoid hemorrhage

- Patients with renal insufficiency

- Patients with acquired disturbances of color vision