Determining Postoperative Recovery and the Impact of Adverse Events in Neurosurgery Based on Self-reported, App-based Longitudinal Assessment

Recruiting Observational Study
Disc Disease Instabilities Lumbar Brain Tumor Aneurysm
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
400 (estimated)
Sponsor
Cantonal Hospital of St. Gallen · Other
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About This Trial
Analyzing the impact of surgery and adverse events (AEs) on patients' well-being is of paramount importance as it provides essential information for benefit-risk assessment. Current methods in outcome research are static, resource-intensive and subject to missing-data issues. Moreover, AEs are inconsistently reported using various grading systems that usually do not account for patients' subjectiv…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age ≥ 18 years * The patient must be able to consent * The patient is willing to provide data upon one year after surgery * The patient possesses and is capable of using a smartphone (Android or iOS operative systems) * The patient has the necessary language and cognitive skil…
Contacts

Alexis PR Terrapon, MD

+41 31 632 24 09

alexis.terrapon@insel.ch

CONTACT

Martin N Stienen, PD Dr

+41 71 494 77 77

martin.stienen@kssg.ch

CONTACT