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Clinical Trials/NL-OMON54782
NL-OMON54782
Recruiting
Phase 4

Prevention of neuropsychiatric adverse effects caused by dexamethasone: insights from a placebo-controlled trial with hydrocortisone. - DEXA-CORT

eids Universitair Medisch Centrum0 sites180 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
eids Universitair Medisch Centrum
Enrollment
180
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Cranial glioma, meningioma or brain metastasis scheduled to undergo surgery
  • (resection)
  • \- Minimal dose of peri\-operative cumulative dexamethasone of 24mg or more in 6
  • \- \>\=18 years
  • \- Good clinical condition; KPS\>\=70
  • \- Life expectancy \>\=6 months

Exclusion Criteria

  • \- Non\-native speakers of Dutch or insufficient command of the Dutch language
  • \- Patients that are unable to overview consequences of trial participation
  • \- Patients with severe aphasia
  • \- Patients that are not able to fill in the questionnaires because of cognitive
  • impairments at the discretion of the physician
  • \- Patients with psychiatric diseases or neurological deficits that interfere
  • with the study to the judgement of treating physician

Outcomes

Primary Outcomes

Not specified

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