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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04870684
Other study ID # 2021-A00171-40
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 1, 2021
Est. completion date May 1, 2024

Study information

Verified date April 2021
Source University Hospital, Caen
Contact Clémence h Tomadessos
Phone +33231065386
Email tomadesso-c@chu-caen.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In ischemic stroke, the recanalization rate after intravenous thrombolysis has been estimated to be less than 50% in patients with proximal intracranial artery occlusion; this rate is greater than 80% after endovascular thrombectomy. Thromboelastometry is a method of analysis of coagulation and fibrinolysis in whole blood. The main objective of this study is to evaluate whether the parameters obtained by thromboelastometry are predictive of revascularization at arteriography during mechanical thrombectomy, after treatment with rt-PA thrombolysis.


Description:

This is a single-center prospective observational study at the University Hospital of Caen. Any patient presenting a neurological deficit of sudden onset, compatible with a ischemic stroke diagnosed on brain imaging and eligible for thrombolysis by rtPA and/or a endovascular thrombectomy procedure will be included. Clot formation kinetics will be assessed by thromboelastometry (ROTEM® and/or QUANTRA®) to determine the predictive parameters of revascularization. The parameters of clot formation and lysis as well as revascularization according to thrombo-inflammation processes will be studied.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date May 1, 2024
Est. primary completion date April 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age > 18 years - Diagnosis of ischemic stroke - Decision of intravenous thrombolysis and/or endovascular thrombectomy by the neurologist and/or interventional neuroradiologist. - Patient admitted to the emergency department during the hours and days when the hematology-biology laboratory is open (Monday to Friday from 8:30 a.m. to 6:30 p.m.) - No opposition to the research from the patient or his relatives - Inclusions according to the emergency procedure Exclusion Criteria: - Age < 18 ans - Formal contraindication to thrombolysis and/or endovascular thrombectomy, disorders of hemostasis and anticoagulant treatment.

Study Design


Intervention

Other:
thromboelastometry test
This study does not modify the usual care of the patient. Only 5 citrated tubes (maximum 15 mL of blood) are collected in addition to the initial emergency department sample (routine care). The patient's care follows the classic thrombolysis alert pathway. There is no additional complementary examination or additional neurological evaluation. Clot formation kinetics will be evaluated by thromboelastometry to determine the predictive parameters of revascularization. Clot formation and lysis parameters as well as revascularization according to thrombo-inflammation processes will be studied.

Locations

Country Name City State
France University hospital of Caen, emergency department Caen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prediction of the success of the revascularization procedure by thromboelastometry All the parameters of clot formation and lysis will be studied, in particular the area under the curve (AUC) One hour after the blood test
Primary Does clot firmness could predict the success of the revascularization clot firmness (MCF in millimeter, mm) One hour after the blood test
Primary Prediction of the success of the revascularization procedure by thromboelastometry clot lysis time (seconde). One hour after the blood test
Secondary Thomboelastometry and prediction of thrombolysis + thrombectomy efficacy effectiveness of thrombectomy will be assessed per-arteriogram by the TICI score (Grade 0: no perfusion Grade 1: penetration with minimal perfusion Grade 2: partial perfusion Grade 2A: only partial filling (less than two-thirds) of the entire vascular territory is visualized Grade 2B: complete filling of all of the expected vascular territory is visualized but the filling is slower than normal Grade 3: complete perfusion) during thrombectomy procedure
Secondary Thomboelastometry and prediction of thrombectomy efficacy number of passes required for successful recanalization thrombolysis immediatly after thrombectomy procedure
Secondary Thomboelastometry and prediction of thrombectomy efficacy puncture to recanalization (minute) through study completion, an average of 3 years
Secondary Thomboelastometry and prediction of success of recanalization by thrombectomy alone Effectiveness of thrombectomy will be assessed by the TICI score ((Grade 0: no perfusion Grade 1: penetration with minimal perfusion Grade 2: partial perfusion Grade 2A: only partial filling (less than two-thirds) of the entire vascular territory is visualized Grade 2B: complete filling of all of the expected vascular territory is visualized but the filling is slower than normal Grade 3: complete perfusion) just at the end of thrombectomy procedure
Secondary Prediction of success of thrombolysis presence or absence of a clot on MRI or angioscan "Day 1", "Day 3" after thrombolysis
Secondary Thomboelastometry and prediction of neurological outcome The use of the NIHSS score will allow the neurological evaluation of the patient (at admission and 24h/72h after the recanalization attempt). Neurological outcome, as assessed by the NIHSS score, is considered favorable if the NIHSS score at 24h/72h post-recanalization is equal to 0 or 1 or if there is an improvement in the NIHSS score of at least four points between the admission score and the score at 24h/72h post-recanalization. "D0", "Day 1", "Day 3" after revascularization
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