Perioperative Bleeding and Aspirin Use in Spine Surgery (ASA)
Primary Purpose
Hemorrhage, Thrombosis
Status
Withdrawn
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Acetylsalicylic acid
Sponsored by
About this trial
This is an interventional prevention trial for Hemorrhage focused on measuring Bleeding, Aspirin, Spine, Surgery
Eligibility Criteria
Inclusion Criteria:
- All patients over 18 years old, who are not taking aspirin at the time of operation as part of a current cardiovascular treatment plan, who will undergo spinal surgery from 2016-2019 in the practice of Dr. Eubanks.
Exclusion Criteria:
- Any patient under the age of 18 and/or is already taking anticoagulant therapy for an established cardiovascular disease at the time of surgery as part of a cardiovascular therapy.
Sites / Locations
- University Hospitals Case Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
No Intervention
Experimental
Experimental
Arm Label
No aspirin
Low-dose aspirin
High-dose aspirin
Arm Description
Patients will not be given any Acetylsalicylic acid in the perioperative period.
Patients will be given low-dose Acetylsalicylic acid (81 mg) in the perioperative period.
Patients will be given high-dose Acetylsalicylic acid (325 mg) in the perioperative period.
Outcomes
Primary Outcome Measures
Hemorrhage: Amount of blood loss
Amount of blood loss from the operation will be recorded
Hemorrhage: Amount of blood loss
Blood loss from drainage tube when applicable
Secondary Outcome Measures
Blood Transfusion: Amount of blood products transfused
Amount of blood products transfused when applicable
Full Information
NCT ID
NCT02807441
First Posted
June 14, 2016
Last Updated
October 3, 2021
Sponsor
University Hospitals Cleveland Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT02807441
Brief Title
Perioperative Bleeding and Aspirin Use in Spine Surgery
Acronym
ASA
Official Title
Association Between Perioperative Bleeding and Aspirin Use in Spine Surgery: A Randomized, Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Withdrawn
Study Start Date
July 2016 (undefined)
Primary Completion Date
July 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospitals Cleveland Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators would like to further the current understanding of aspirin and its effects on perioperative bleeding by conducting a randomized controlled trial of spinal surgery patients receiving varying doses of aspirin or no aspirin perioperatively. The investigators hypothesize that there will be no significant difference in perioperative blood loss between the different groups.
Detailed Description
Selected patients will be given either no aspirin, low-dose aspirin (81 mg), or high-dose aspirin (325 mg) in the perioperative period. These dosages are based on the Pharmacist's letter/Prescriber's letter which provides aspirin dosing recommendations for varying cardiovascular indications. Allocation of dosing will be based on computerized randomization in order to achieve approximately 100 patients in each group. Patient records will then be assessed for demographic characteristics, comorbidities, symptoms, functional outcome scores (Sf-12), operative time, intraoperative estimated blood loss, postoperative blood loss in drainage tubes (when applicable), cumulative blood loss, transfusion of blood products, hemoglobin level, preoperative International Normalized Ratio (INR), preoperative platelet count, hospital length of stay, and morbidity and mortality including development of NSTEMI, atrial fibrillation, surgical site infection, pulmonary embolism, and hospital 30-day readmission rates.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhage, Thrombosis
Keywords
Bleeding, Aspirin, Spine, Surgery
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
No aspirin
Arm Type
No Intervention
Arm Description
Patients will not be given any Acetylsalicylic acid in the perioperative period.
Arm Title
Low-dose aspirin
Arm Type
Experimental
Arm Description
Patients will be given low-dose Acetylsalicylic acid (81 mg) in the perioperative period.
Arm Title
High-dose aspirin
Arm Type
Experimental
Arm Description
Patients will be given high-dose Acetylsalicylic acid (325 mg) in the perioperative period.
Intervention Type
Drug
Intervention Name(s)
Acetylsalicylic acid
Other Intervention Name(s)
aspirin
Intervention Description
Patients will receive different doses of aspirin perioperatively to assess bleeding association.
Primary Outcome Measure Information:
Title
Hemorrhage: Amount of blood loss
Description
Amount of blood loss from the operation will be recorded
Time Frame
Intraoperative
Title
Hemorrhage: Amount of blood loss
Description
Blood loss from drainage tube when applicable
Time Frame
48 hours Postoperative
Secondary Outcome Measure Information:
Title
Blood Transfusion: Amount of blood products transfused
Description
Amount of blood products transfused when applicable
Time Frame
Intraoperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
All patients over 18 years old, who are not taking aspirin at the time of operation as part of a current cardiovascular treatment plan, who will undergo spinal surgery from 2016-2019 in the practice of Dr. Eubanks.
Exclusion Criteria:
Any patient under the age of 18 and/or is already taking anticoagulant therapy for an established cardiovascular disease at the time of surgery as part of a cardiovascular therapy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jason Eubanks, MD
Organizational Affiliation
University Hospitals Cleveland Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospitals Case Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data will be collected on a computer database containing unique identifiers, without names, social security numbers, medical record numbers, or other information that could be used to identify individuals. University Hospitals Research Electronic Data Capture will be used as a means of secure data storage. At no time will this data spreadsheet be printed or otherwise distributed, and no Protected Health Information will be transferred to investigators at other sites of this multi-center study.
Citations:
PubMed Identifier
21212258
Citation
Hall R, Mazer CD. Antiplatelet drugs: a review of their pharmacology and management in the perioperative period. Anesth Analg. 2011 Feb;112(2):292-318. doi: 10.1213/ANE.0b013e318203f38d. Epub 2011 Jan 6.
Results Reference
background
PubMed Identifier
26030214
Citation
Cuellar JM, Petrizzo A, Vaswani R, Goldstein JA, Bendo JA. Does aspirin administration increase perioperative morbidity in patients with cardiac stents undergoing spinal surgery? Spine (Phila Pa 1976). 2015 May 1;40(9):629-35. doi: 10.1097/BRS.0000000000000695.
Results Reference
background
PubMed Identifier
22470078
Citation
Gerstein NS, Schulman PM, Gerstein WH, Petersen TR, Tawil I. Should more patients continue aspirin therapy perioperatively?: clinical impact of aspirin withdrawal syndrome. Ann Surg. 2012 May;255(5):811-9. doi: 10.1097/SLA.0b013e318250504e.
Results Reference
background
PubMed Identifier
25757534
Citation
Soleman J, Baumgarten P, Perrig WN, Fandino J, Fathi AR. Non-instrumented extradural lumbar spine surgery under low-dose acetylsalicylic acid: a comparative risk analysis study. Eur Spine J. 2016 Mar;25(3):732-9. doi: 10.1007/s00586-015-3864-7. Epub 2015 Mar 11.
Results Reference
background
PubMed Identifier
25695574
Citation
Gerstein NS, Carey MC, Cigarroa JE, Schulman PM. Perioperative aspirin management after POISE-2: some answers, but questions remain. Anesth Analg. 2015 Mar;120(3):570-575. doi: 10.1213/ANE.0000000000000589.
Results Reference
background
PubMed Identifier
23615883
Citation
Manchikanti L, Abdi S, Atluri S, Benyamin RM, Boswell MV, Buenaventura RM, Bryce DA, Burks PA, Caraway DL, Calodney AK, Cash KA, Christo PJ, Cohen SP, Colson J, Conn A, Cordner H, Coubarous S, Datta S, Deer TR, Diwan S, Falco FJ, Fellows B, Geffert S, Grider JS, Gupta S, Hameed H, Hameed M, Hansen H, Helm S 2nd, Janata JW, Justiz R, Kaye AD, Lee M, Manchikanti KN, McManus CD, Onyewu O, Parr AT, Patel VB, Racz GB, Sehgal N, Sharma ML, Simopoulos TT, Singh V, Smith HS, Snook LT, Swicegood JR, Vallejo R, Ward SP, Wargo BW, Zhu J, Hirsch JA. An update of comprehensive evidence-based guidelines for interventional techniques in chronic spinal pain. Part II: guidance and recommendations. Pain Physician. 2013 Apr;16(2 Suppl):S49-283.
Results Reference
background
PubMed Identifier
24740280
Citation
Park HJ, Kwon KY, Woo JH. Comparison of blood loss according to use of aspirin in lumbar fusion patients. Eur Spine J. 2014 Aug;23(8):1777-82. doi: 10.1007/s00586-014-3294-y. Epub 2014 Apr 17.
Results Reference
background
PubMed Identifier
21474081
Citation
Kang SB, Cho KJ, Moon KH, Jung JH, Jung SJ. Does low-dose aspirin increase blood loss after spinal fusion surgery? Spine J. 2011 Apr;11(4):303-7. doi: 10.1016/j.spinee.2011.02.006.
Results Reference
background
PubMed Identifier
26620144
Citation
Wong SS, Irwin MG. Peri-operative cardiac protection for non-cardiac surgery. Anaesthesia. 2016 Jan;71 Suppl 1:29-39. doi: 10.1111/anae.13305.
Results Reference
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Perioperative Bleeding and Aspirin Use in Spine Surgery
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