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Clinical Trials/DRKS00013047
DRKS00013047
Completed
未知

Intraoperative neuromonitoring of neurosurgical patients using a non-invasive tissue-photospectrometry technique

eurochirurgische Klinik, Universitätsklinikum Erlangen0 sites74 target enrollmentOctober 2, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
cerebral aneurysm, intracranial hemorrhage, cerebral ischemia, brain edema
Sponsor
eurochirurgische Klinik, Universitätsklinikum Erlangen
Enrollment
74
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 2, 2017
End Date
October 21, 2017
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
eurochirurgische Klinik, Universitätsklinikum Erlangen

Eligibility Criteria

Inclusion Criteria

  • a) All participants of this study have to be either fully competent or provide a legal guardian for medical concerns
  • b) Written informed consent of the participant or his/her legal guardian
  • c) Age of 18 to 85 years, both genders.
  • d) Depending on the study phase, two groups are investigated:
  • Group 1: Patients undergoing a scheduled neurosurgical operation such as resection of a supra\- or infratentorial lesion (meningeoma, vestibular schwannoma, pituitary adenoma, arachnoid cyst)
  • Group 2: Patients with life\-threatening neurosurgical disease which requires emergency surgery within 72 hours such as intracranial hemorrhage or brain tumors with mass effect.

Exclusion Criteria

  • a) decompensated liver\- or renal disease
  • b) acute coronary syndrome
  • c) severe comorbidity (mRS \= 3\)
  • d) pregnancy
  • e) last participation in a trial \<6 months

Outcomes

Primary Outcomes

Not specified

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