Overview
Does Tranexamic Acid Improve Visualization During Arthroscopic Rotator Cuff Repair
Status:
Recruiting
Recruiting
Trial end date:
2022-04-01
2022-04-01
Target enrollment:
0
0
Participant gender:
All
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 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University of SaskatchewanTreatments:
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