Syncope Clinical Trial
Official title:
Lactate Compared to Creatine Kinase as Diagnostic Marker in Generalized Epileptic Seizure
The investigators compared the feasibility of serum creatine kinase and serum lactate concentration as diagnostic markers to distinguish between generalized tonic-clonic seizures (GTCS) and syncopes in clinical settings that require fast-action treatment, such as in the emergency departments.
The patients of this prospective study were selected from a sample of patients who were
admitted to the emergency room of the University Hospital RWTH Aachen with an unclear
impairment of consciousness. Only patients who later on were diagnosed as having experienced
a GTCS or a syncope and whose serum lactate concentrations had been measured within 2 hours
after the event were enrolled in the study. The investigators compared the specificity and
sensitivity of the serum lactate concentrations at admission with the CK concentration at
admission and the CK follow-up taken 10 to 48 hours after the event.
The values at admission were compared between patients from whom a blood sample was
collected within 60 minutes after the event, and those from whom a blood sample was
collected within 61-120 minutes after the event.
The comparison of initial lactate concentrations at admission with CK levels 10 - 48 hours
later could only be performed on part of the patient collective because the other patients
were already discharged at this time-point and could therefore not be included.
The initial blood samples were taken at patient arrival in the emergency room. The follow up
was performed during the inpatient stay.
Serum lactate and CK concentrations between patient groups were statistically compared with
a Mann-Whitney-U test. We defined cut-off values and their sensitivity and specificity by
Receiver Operating Characteristic (ROC) analysis.
;
Observational Model: Cohort, Time Perspective: Prospective
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT06038708 -
Head-up Tilt Test in Patients With Reflex Syncope and Asystolic Response Who Received a Dual-chamber Pacemaker With the Closed Loop Stimulation (CLS) and Participated in the BIOSync Trial
|
||
Completed |
NCT00069693 -
Evaluation of Chronic Orthostatic Intolerance
|
N/A | |
Not yet recruiting |
NCT05649891 -
Checklists Resuscitation Emergency Department
|
N/A | |
Completed |
NCT02565238 -
BIO.MASTER.BioMonitor 2 Study
|
N/A | |
Active, not recruiting |
NCT01965899 -
Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System
|
N/A | |
Completed |
NCT00746564 -
Study of New Implantable Loop Recorder
|
N/A | |
Completed |
NCT00359203 -
ISSUE3: International Study on Syncope of Uncertain Etiology 3
|
Phase 4 | |
Recruiting |
NCT04972071 -
SW-RCT Implementation of Canadian Syncope Risk Score Based Practice Recommendations
|
N/A | |
Completed |
NCT04198220 -
BIO|STREAM.ICM Obesity
|
||
Recruiting |
NCT04533425 -
Practical Approaches to Care in Emergency Syncope
|
||
Completed |
NCT05571254 -
The Management of Transient Loss of Consciousness and Suspected Syncope in European Emergency Departments
|
||
Recruiting |
NCT05621460 -
The Effect of Water Carbonation on Orthostatic Tolerance
|
N/A | |
Not yet recruiting |
NCT05957315 -
Mobile Cardiac Outpatient Telemetry for Unexplained Syncope
|
N/A | |
Recruiting |
NCT04615065 -
Acutelines: a Large Data-/Biobank of Acute and Emergency Medicine
|
||
Completed |
NCT05729724 -
Effect of Pharmacological Interventions on Systolic Blood Pressure Drops (SynABPM 2 Proof-of-concept)
|
||
Completed |
NCT05782712 -
Rapid Measurement of Adenosine in Syncope Patients
|
||
Completed |
NCT03786640 -
Abbott Brady 3T MRI PMCF
|
||
Recruiting |
NCT03803969 -
ConfirmRxTM: Posture and Activity
|
N/A | |
Recruiting |
NCT05575934 -
Management of Transitory Loss of Consciousness and Syncopes in the Emergency Department
|
||
Recruiting |
NCT04075084 -
Observation of Clinical Routine Care for Patients With BIOTRONIK Implantable Cardiac Monitors (ICMs)
|