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Clinical Trials/NL-OMON42478
NL-OMON42478
Completed
N/A

Orthostatic related blood pressure changes in syncope patients in the emergency department - Orthostatic blood pressure

Acute interne geneeskunde0 sites100 target enrollmentTBD
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ConditionsSyncopefaintingloss of consciusness10011954

Overview

Phase
N/A
Intervention
Not specified
Conditions
Syncope
Sponsor
Acute interne geneeskunde
Enrollment
100
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Acute interne geneeskunde

Eligibility Criteria

Inclusion Criteria

  • •The patient must be 18 years or older.
  • •The reason for referral to the emergency department must be (pre\-) syncope.
  • •The patient must be able to stand for 5 minutes with little assistance.

Exclusion Criteria

  • •The patient is not able to stand for 5 minutes (with little assistance)
  • •The patient is hemodynamically instable (with supine resting SBP \<90 mmHg or DBP \<50 mmHg)
  • •The patient needs immediate additional investigations/treatment
  • •The patient is psychologically, physically (due to any other illness) or cognitively unfit for participation in the study according to the opinion of the investigator
  • •The patient has a MMSE score \<21 during the first outpatient clinic visit
  • •The patient is geographically or otherwise inaccessible to follow up
  • •The patient is unwilling or unable to give informed consent
  • •The patient has atrial fibrillation in the emergency department
  • •When there are other reasons for transient loss of consciousness, which do not fit the definition of syncope, such as alcohol, illicit drugs, seizure, stroke/transient ischemic attack, head trauma or hypoglycemia
  • •Life expectancy \< 1 year

Outcomes

Primary Outcomes

Not specified

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