search
Back to results

STRATAGEM: Strategy for Managing Antiplatelet Therapy in the Perioperative Period of Non Coronary Surgery (STRATAGEM)

Primary Purpose

Thrombosis

Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
aspirin 75 mg/day
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Thrombosis focused on measuring Long term antiplatelet therapy, Scheduled surgery

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Written informed consent Patients over eighteen years of age Patients treated with oral antiplatelet agents for secondary prevention (i.e. established and symptomatic cardiovascular disease): regardless of the reason (coronary artery disease, stroke or TIA [transient ischemic attack], peripheral arterial disease) regardless of the antiplatelet agent (aspirin, clopidogrel, ticlopidine, dipyridamole). Patients scheduled for intermediate or high-risk surgery, including but not limited to: any long procedure associated with hemodynamic variations or major blood loss valvular surgery thoracic surgery orthopedic surgery general (intraperitoneal) surgery urological surgery vascular surgery ear, nose, and throat (ENT) cancerology-related surgery. Exclusion Criteria: Coronary bypass grafting surgery History of thrombocytopenia or allergy to heparin Arterial stent placement within the previous 30 days Active bleeding Formal contraindication to the use of anticoagulants and aspirin Recent acute coronary syndrome Ophthalmological surgery (posterior chamber) Neurosurgery Emergency surgery Thrombotic or bleeding risk deemed unacceptable by the surgical and anesthetic team Pregnancy

Sites / Locations

  • Hôpital Beaujon

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Aspirin:KARDEGIC

Outcomes

Primary Outcome Measures

Consisting of major thromboembolic events listed in the following table with their respective weights.
The score allocated to each patient is the weight of the event (zero if no event has occurred). For the patients having experienced more than one event, the score attributed is the "heaviest" weight among the events he has undergone.

Secondary Outcome Measures

Full Information

First Posted
September 12, 2005
Last Updated
September 20, 2011
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Sanofi-Synthelabo
search

1. Study Identification

Unique Protocol Identification Number
NCT00190307
Brief Title
STRATAGEM: Strategy for Managing Antiplatelet Therapy in the Perioperative Period of Non Coronary Surgery
Acronym
STRATAGEM
Official Title
Strategy for Managing Antiplatelet Therapy in the Perioperative Period of Non Coronary Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
September 2005
Overall Recruitment Status
Completed
Study Start Date
June 2005 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Sanofi-Synthelabo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The STRATAGEM trial is an investigator-driven French nationwide multicenter, randomized, double-blind, placebo-controlled trial comparing perioperative low-dose aspirin therapy versus placebo in the perioperative period in patients with documented symptomatic stable atherothrombotic disease taking antiplatelet therapy and undergoing non-coronary surgery.
Detailed Description
There is little evidence to guide antiplatelet therapy in patients at high risk of atherothrombotic events undergoing non cardiac surgery. Specifically, it is uncertain whether patients currently on antiplatelet therapy should continue or not continue treatment in the perioperative period. Aim: To determine an evidence-based strategy for managing antiplatelet therapy in the perioperative period. Methods: The STRATAGEM trial is an investigator-driven French nationwide multicenter, randomized, double-blind, placebo-controlled trial comparing perioperative low-dose aspirin therapy versus placebo in the perioperative period in patients with documented symptomatic stable atherothrombotic disease taking antiplatelet therapy and undergoing non-coronary surgery. The trial will involve 1500 patients at high risk of atherothrombosis, currently receiving long-term antiplatelet therapy and scheduled for non-coronary surgery in 50 centers. Ten days prior to surgery, patients will discontinue antiplatelet therapy and be randomly assigned to either 75 mg of aspirin or matching placebo for 10 days up to the surgical procedure. Usual therapy will be resumed after surgery according to local practice. The main outcome measure will be a composite endpoint at day 30 reflecting serious perioperative complications, i.e. total mortality, severe ischemic events (ischemic stroke, non-fatal myocardial infarction [MI], acute limb ischemia, clinical deep venous thrombosis) and/or major hemorrhage (life-threatening bleeding or conducive to revision, or redo surgery, cerebral hemorrhage, intra- or retroperitoneal bleeding, bleeding resulting in the transfusion of more than 2 units of packed red blood cells). The hypothesis to be tested is that low-dose aspirin is associated with a net clinical benefit compared to placebo in the prevention of severe perioperative thrombotic and hemorrhagic complications.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thrombosis
Keywords
Long term antiplatelet therapy, Scheduled surgery

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
293 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Aspirin:KARDEGIC
Intervention Type
Drug
Intervention Name(s)
aspirin 75 mg/day
Intervention Description
aspirin 75 mg/day
Primary Outcome Measure Information:
Title
Consisting of major thromboembolic events listed in the following table with their respective weights.
Description
The score allocated to each patient is the weight of the event (zero if no event has occurred). For the patients having experienced more than one event, the score attributed is the "heaviest" weight among the events he has undergone.
Time Frame
A composite criterion measured at Day 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Written informed consent Patients over eighteen years of age Patients treated with oral antiplatelet agents for secondary prevention (i.e. established and symptomatic cardiovascular disease): regardless of the reason (coronary artery disease, stroke or TIA [transient ischemic attack], peripheral arterial disease) regardless of the antiplatelet agent (aspirin, clopidogrel, ticlopidine, dipyridamole). Patients scheduled for intermediate or high-risk surgery, including but not limited to: any long procedure associated with hemodynamic variations or major blood loss valvular surgery thoracic surgery orthopedic surgery general (intraperitoneal) surgery urological surgery vascular surgery ear, nose, and throat (ENT) cancerology-related surgery. Exclusion Criteria: Coronary bypass grafting surgery History of thrombocytopenia or allergy to heparin Arterial stent placement within the previous 30 days Active bleeding Formal contraindication to the use of anticoagulants and aspirin Recent acute coronary syndrome Ophthalmological surgery (posterior chamber) Neurosurgery Emergency surgery Thrombotic or bleeding risk deemed unacceptable by the surgical and anesthetic team Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Mantz, MD
Organizational Affiliation
Hôpital Beaujon, Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Beaujon
City
Clichy
ZIP/Postal Code
92110
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
21873632
Citation
Mantz J, Samama CM, Tubach F, Devereaux PJ, Collet JP, Albaladejo P, Cholley B, Nizard R, Barre J, Piriou V, Poirier N, Mignon A, Schlumberger S, Longrois D, Aubrun F, Farese ME, Ravaud P, Steg PG; Stratagem Study Group. Impact of preoperative maintenance or interruption of aspirin on thrombotic and bleeding events after elective non-cardiac surgery: the multicentre, randomized, blinded, placebo-controlled, STRATAGEM trial. Br J Anaesth. 2011 Dec;107(6):899-910. doi: 10.1093/bja/aer274. Epub 2011 Aug 27.
Results Reference
result

Learn more about this trial

STRATAGEM: Strategy for Managing Antiplatelet Therapy in the Perioperative Period of Non Coronary Surgery

We'll reach out to this number within 24 hrs