Hemostasis Profile in Patients With Severe Subarachnoid Hemorrhage

• ClinicalTrials.gov Identifier: NCT03745456
• Recruitment Status: Unknown
• First Posted: November 19, 2018
• Last Update Posted: December 4, 2018
• Sponsor: Hospitales Universitarios Virgen del Rocío
• Information provided by (Responsible Party): Santiago R. Leal-Noval, Hospitales Universitarios Virgen del Rocío

Study Description

Brief Summary:

Patients with severe subarachnoid hemorrhage (SAH) may present platelet and coagulation dysfunctions immediately after the stroke on admission at the hospital, and persisting up to 3-4 weeks after the onset. This study aimed to investigate the platelet function as assessed by impedance agregometry (ROTEM Platelet) and platelet adhesion (PFA), and the coagulation profile as assessed by ROTEM, over three evolutive times.

Condition or disease	Intervention/treatment
Subarachnoid Hemorrhage; Platelet Dysfunction; Coagulation Disorder	Diagnostic Test: Blood samples for ROTEM and platelet function.

Detailed Description:

Patients with severe subarachnoid hemorrhage (SAH) present platelet and coagulation dysfunctions immediately after the stroke, at least two weeks after the onset of SAH. These alterations have been implicated in the presentation of delayed cerebral ischemia (DCI), vasospasm, deep vein thrombosis (DVT) and long-term neurological deterioration. The temporal presentation of the platelet dysfunction and coagulation has not consistently been established, nor have they been assessed with tests for specific platelet receptors. Objective. Primary: To document the platelet function and coagulation, in constant and fixed periods after the stroke onset, in patients with severe SAH, Hunt and Hess 4-5, Fisher 4. Secondary: Relationship between the patterns of hemostasis and coagulation and the presence of vasospasm, DCI and DVT. Method. Prospective, cohort study that will include (calculated sample size) 50 patients with severe SAH, recruited in the first 6 hours after the onset of symptoms. Twenty healthy volunteers (already recruited) will constitute the control group. Platelet function will be studied by platelet count, von Willebrand factor level, platelet function assay (PFA-100), and platelet ROTEM for specific stimulation of platelet receptors (ARATEM, ADPTEM, TRAPTEM). The coagulation will be investigated by conventional coagulation study, ROTEM EXTEM, ROTEM FIBTEM and factor XIII. In the group with SAH, blood samples will be drawn into the first 6 hours after the onset of symptoms (t0), in the period of 8 - 10 days after the stroke (t1) - period of maximum incidence of TBI and DVT - and 14- 16 days after the stroke (t2) in order to evaluate the late degree of coagulation alterations. Baseline values (t0) will be compared between subjects with HSA and the control group (intersubjects comparisons.). On the other hand, significant changes of the hemostasis and coagulation values among the times t0, t1 and t2 in the HAS group, will be also investigated (intra-subjects comparisons). Additionally, the relationship between the hemostasis and coagulation values evaluated at any of the specified time and the clinical outcome, as assessed by the presence of DCI, vasospasm, DVT or neurological deterioration at 3 months of follow-up (mRs> 3), will be also investigated

Study Design

• Study Type: Observational
• Estimated Enrollment: 50 participants
• Observational Model: Case-Only
• Time Perspective: Prospective
• Official Title: Hemostasis Profile in Patients With Severe Subarachnoid Hemorrhage
• Estimated Study Start Date: December 1, 2018
• Estimated Primary Completion Date: December 1, 2019
• Estimated Study Completion Date: July 1, 2020

Groups and Cohorts

Group/Cohort	Intervention/treatment
Subarachnoid Hemorrhage patients; Patients with severe subarachnoid hemorrhage (Hunt and Hess 4-5, Fisher 3-4) will be included initially in the first 6 hours after the onset of symptoms.	Diagnostic Test: Blood samples for ROTEM and platelet function.; Thormoboelastometry is based on the measurement of elasticity of blood by continuous graphical logging of the firmness of a blood clot during clot formation and subsequent fibrinolysis

Outcome Measures

Primary Outcome Measures :

1. ROTEM, ROTEM platelet and PFA variations in patients wit SAH. [ Time Frame: 1 month. ]
   Document the platelet function (ROTEM platelet and PFA) and coagulation (ROTEM), in constant and fixed periods after the presentation of the stroke, in patients with severe SAH, defined by Hunt and Hess 4-5, Fisher 3-4.

Secondary Outcome Measures :

1. Secondary outcomes [ Time Frame: 6 months ]
   Relationship between hemostasis and coagulation patterns and the presence of vasospasm, Late Cerebral Ischemia and Deep Venous Thrombosis

Biospecimen Retention:   Samples Without DNA

Blood samples for coagulation profile (ROTEM and clotting tests) and platelet function (ROTEM platelet and PFA)

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No
• Sampling Method: Non-Probability Sample

Study Population

Patients with severe subarachnoid hemorrhage (Hunt and Hess 4-5, Fisher 3-4) in the first 6 hours after the onset of symptoms

Criteria

Inclusion Criteria:

• Consecutive patients with severe subarachnoid hemorrhage (Hunt and Hess 4-5, Fisher 3-4) will be included initially in the first 6 hours after the onset of symptoms.

Exclusion Criteria:

1. Patient with known coagulopathy or with ingestion of antiplatelet drugs or anticoagulants in the 15 days prior to the presentation of symptoms.
2. Patients in whom there is no confirmed arteriovenous malformation.
3. The patient or authorized family member denies informed consent.
4. High risk of imminent death, evaluated by the doctor in charge of the patient.
5. Hemoglobin <100 g / L and / or platelet count <100,000 microL

Contacts and Locations

Contacts

Contact: Santiago R leal-Noval, MD; +00 34 955012528 ext 312528; srlealnoval@gmail.com

Locations

Spain

Hospital Universitario "Virgen del Rocío"

Seville, Spain, 41013

Sponsors and Collaborators

Hospitales Universitarios Virgen del Rocío

Investigators

• Principal Investigator: Santiago R Leal-Noval, MD; Medical staff of Neuro Critical Care

More Information

• Responsible Party: Santiago R. Leal-Noval, Senior, Hospitales Universitarios Virgen del Rocío
• ClinicalTrials.gov Identifier: NCT03745456
• Other Study ID Numbers: HUVRocio
• First Posted: November 19, 2018
• Last Update Posted: December 4, 2018
• Last Verified: December 2018

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: Undecided

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Santiago R. Leal-Noval, Hospitales Universitarios Virgen del Rocío:

Rotational Thromboelstrometry

Additional relevant MeSH terms:

Subarachnoid Hemorrhage; Hemostatic Disorders; Blood Coagulation Disorders; Hemorrhage; Pathologic Processes; Intracranial Hemorrhages; Cerebrovascular Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases; Hematologic Diseases; Hemorrhagic Disorders