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Cardiopulmonary Complication in Aneurysmal Subarachnoid Haemorrhage Patients

Cardiopulmonary Complication in Aneurysmal Subarachnoid Haemorrhage Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01670838
Acronym
SAHHEART
Enrollment
198
Registered
2012-08-22
Start date
2012-02-29
Completion date
2017-08-31
Last updated
2018-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aneurysmal Subarachnoid Heamorrhage, Nontraumatic Subarachnoid Haemorrhage

Keywords

subarachnoid haemorrhage, cardiopulmonary complications

Brief summary

This is a prospective cohort study investigating cardiac function and cardiac biomarkers in patients with acute Aneurysmal Subarachnoid Haemorrhage (aSAH). The aims of the study are to document the incidence of myocardial dysfunction,to find the predictive factors of myocardial dysfunction, describe heart rate variability and to assess the impact of all cardiac problems on morbidity and mortality.

Detailed description

Laboratory markers daily: Routine laboratory test (blood gases, haemoglobin, thrombocytes, leukocytes, INR, bilirubin, creatinine, c-reactive protein, CK, CK-MB, Tnt, BNP, sodium, potassium, magnesium) are taken at 8 a.m. Study laboratory tests (sensitive ischemia markers, remodelling marker MMP-9 and CgA as surrogate marker for increased sympathetic activity) are taken four times during study period at the same time as cardiac ECHOes and Holtering. Gene sample is taken once on day one. Primary outcome measurement is to document the incidence of myocardial dysfunction and the predictive factors during the hospital stay and at three months. Secondary outcome is to assess the impact of cardiac problems on morbidity and mortality during first three months.

Interventions

None listed

Sponsors

Turku University Hospital
CollaboratorOTHER_GOV
Kuopio University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with nontraumatic subarachnoid haemorrhage * Age \> 18 years * Aneurysmal bleeding

Exclusion criteria

* No consent * Age \< 18 years * Anticipated brain death \< 24 hours * Otherwise moribund patient

Design outcomes

Primary

MeasureTime frameDescription
Incidence of cardiac failure and the impact of cardiac problems on morbidity6 monthsThe aims of the study are: 1. to document the incidence of myocardial dysfunction 2. to find the predictive factors of myocardial dysfunction as determined by the severity aneurysmal bleeding (Hunt and Hess-grading, Glasgow coma score, Fisher scale) and demographic factors 3. to find predictive factors for myocardial dysfunction as determined by laboratory findings, electrocardiography, and echocardiography 4. to describe heart rate variability 5. to assess the impact of all cardiac problems on morbidity

Countries

Finland, Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026