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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03245866
Other study ID # SwissSOS_0001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2009
Est. completion date December 31, 2030

Study information

Verified date May 2023
Source University Hospital, Geneva
Contact Karl Schaller, MD
Phone +41223728202
Email karl.schaller@hcuge.ch
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This registry was created to assess management parameters of patients treated for aneurysmal subarachnoid hemorrhage in Switzerland. All Swiss hospitals with a neurosurgery department, an intensive care unit and an interventional neuroradiology team that treat neurovascular emergencies participate in the registry. Clinical parameters are entered into a common database. This database will provide (1) a nationwide assessment of the current standard of care and (2) the outcomes for patients in Switzerland including neuropsychological assessments.


Description:

Overview: The management of aneurysmal subarachnoid hemorrhage (aSAH) in Switzerland has not been assessed on a national level to date. The investigators united all comprehensive neurovascular care centres in Switzerland to create a registry for aSAH. This registry helps collect clinical and management data from different centres and pools it in one common database. It may provide referring caregivers and healthcare providers with a critical tool to assess the quality of care in a disease which has a high socio-economic burden. Moreover, it may serve as a tool to foster scientific collaboration and address a number of remaining questions about the management of aSAH in the future. Regarding SAH, data from the federal statistics bureau of Switzerland are based strictly on ICD-10 codes provided by hospitals and show an estimate of 13 per 100,000 in a population of roughly 8 million (http://bfs.admin.ch). These numbers, however, are not referring to aneurismal SAH exclusively and thus exceed the numbers which the investigators expect to obtain. The goal is to obtain complete recruitment of SAH patients throughout Switzerland, and the goal is therefore that assessment of incidence will be performed later on. Data management: Data is entered into a central online database created by the Secutrial platform. This platform is provided by the University Hospital of Geneva's Clinical Research Unit. The database disposes of an audit-trail capacity. Local principal investigators are responsible for data-cross check and quality management. Source data verification is performed by investigators on site who address missing data. Regular meetings are held to discuss data patency. The platform automatically provides a report on recruitment progress.


Recruitment information / eligibility

Status Recruiting
Enrollment 5000
Est. completion date December 31, 2030
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion criteria: - Patients admitted with a proven diagnosis of aneurysmal subarachnoid hemorrhage. Exclusion criteria: - Patients in whom the source of haemorrhage could not be identified (angiogram-negative SAH) or SAH with other causes than cerebral aneurysms.

Study Design


Intervention

Other:
Observational/ no intervention


Locations

Country Name City State
Switzerland Kantonsspital Aarau Aarau Aargau
Switzerland University Hospital Basel Basel
Switzerland University Hospital Bern Bern
Switzerland Geneva University Hospital Geneva GE
Switzerland University Hospital Lausanne Lausanne
Switzerland Ospedale Civico Lugano
Switzerland Luzerner Kanton Spital Luzern
Switzerland Kantonsspital St. Gallen St. Gallen Saint Gallen
Switzerland University Hospital Zürich Zürich

Sponsors (8)

Lead Sponsor Collaborator
University Hospital, Geneva Cantonal Hospital of St. Gallen, Kantonsspital Aarau, Ospedale Regionale di Lugano, University Hospital, Basel, Switzerland, University Hospital, Zürich, University of Bern, University of Lausanne Hospitals

Country where clinical trial is conducted

Switzerland, 

References & Publications (2)

Schatlo B, Fung C, Fathi AR, Sailer M, Winkler K, Daniel RT, Bijlenga P, Ahlborn P, Seule M, Zumofen D, Reinert M, Woernle C, Stienen M, Levivier M, Hildebrandt G, Mariani L, Bernays R, Fandino J, Raabe A, Keller E, Schaller K. Introducing a nationwide re — View Citation

Zweifel-Zehnder AE, Stienen MN, Chicherio C, Studerus-Germann A, Blasi S, Rossi S, Gutbrod K, Schmid N, Beaud V, Mondadori C, Brugger P, Sacco L, Muri R, Hildebrandt G, Fournier JY, Keller E, Regli L, Fandino J, Mariani L, Raabe A, Daniel RT, Reinert M, Robert T, Schatlo B, Bijlenga P, Schaller K, Monsch AU; Swiss SOS study group. Call for uniform neuropsychological assessment after aneurysmal subarachnoid hemorrhage: Swiss recommendations. Acta Neurochir (Wien). 2015 Sep;157(9):1449-58. doi: 10.1007/s00701-015-2480-y. Epub 2015 Jul 16. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Functional outcome as assessed by the modified Rankin scale The modified Rankin scale is used to represent the level of disability and is divided into 7 categories (0-6). The scale runs from 0-6, running from perfect health without symptoms to death.
0 - No symptoms.
- No significant disability. Able to carry out all usual activities, despite some symptoms.
- Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities.
- Moderate disability. Requires some help, but able to walk unassisted.
- Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted.
- Severe disability. Requires constant nursing care and attention, bedridden, incontinent.
- Dead.
5 years after hemorrhage
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