Effectiveness Study of the Drug Tranexamic Acid to Reduce Post-surgery Blood Loss in Spinal Surgery
Lumbar Spinal Stenosis, Thoracic Spinal Stenosis
About this trial
This is an interventional supportive care trial for Lumbar Spinal Stenosis focused on measuring lumbar spine surgery, thoracic spine surgery
Eligibility Criteria
Inclusion Criteria:
- 18-85 years, both male and female
- Undergoing elective multi-level spinal surgery with a posterior approach to the thoracolumbar spine.
- Negative pregnancy test
Exclusion Criteria:
- Allergy to tranexamic acid
- Preoperative anemia (Hemoglobin <11 grams per deciliter [g/dL] )
- Coagulopathy (preoperative platelet count <150,000, International Normalized Ratio >1.4, or Partial Thromboplastin Time > 1.5 times normal)
- History of deep vein thrombosis, stroke, or pulmonary embolism
- Pregnant or breast feeding
- Liver function tests 2 times the upper limit of normal, and those with creatine greater than 1.6 milligrams per deciliter (mg/dL)
- Infection
- Revision procedure in which the only procedure is removing instrumentation
- Renal impairment
- Dural tear
Sites / Locations
- Massachusetts General Hospital Orthopedic Spine
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Tranexamic acid
Placebo
Participants undergoing spinal surgery will receive a single, topical dose of tranexamic acid. The surgeon will irrigate the study medication in the wound prior to closure, and aspirate it after five minutes. Drains will be placed after the study drug has been aspirated.
Participants undergoing spinal surgery will receive a single, topical dose of matching placebo. The surgeon will irrigate the study medication in the wound prior to closure, and aspirate it after five minutes. Drains will be placed after the study drug has been aspirated.