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Clinical Trials/NCT03666507
NCT03666507CompletedNot Applicable

Vegetative Monitoring During Brainstem-associated Surgery

University Hospital Tuebingen1 site in 1 country103 target enrollmentStarted: August 28, 2018Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
103
Locations
1
Primary Endpoint
Heart rate variability (HRV)
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Intraoperative Monitoring of Heart rate variability, Blood pressure variability, Baroreceptorsensivity etc.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •brain tumor

Exclusion Criteria

  • •no consent

Outcomes

Primary Outcomes

Heart rate variability (HRV)

Time Frame: intraoperatively

Comparison of HRV in the 2 groups (brain stem-associated vs. non associated surgery)

Secondary Outcomes

  • Rate of cardiovascular complications(intraoperatively)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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Vegetative Monitoring During... | Clinical Trial