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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01123746
Other study ID # 98088
Secondary ID
Status Completed
Phase N/A
First received May 12, 2010
Last updated May 12, 2010
Start date October 2009
Est. completion date April 2010

Study information

Verified date May 2010
Source Taipei Medical University WanFang Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

Objective: To evaluate the predisposing factors associated with abnormal laboratory findings in patients who came to the emergency room due to a first seizure.

Methods: Patients were divided into separate groups based on normal and abnormal laboratory results for sodium, potassium, calcium, and glucose. The difference in age, gender, whether this was the first attack, whether there was fever, whether there were gastrointestinal symptoms, the duration and pattern of the seizure, and whether there was a seizure at the emergency department, were evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date April 2010
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- Age: less than 18 years old

- The patient came to emergency department due to seizure

- The patient received blood sampling including serum sodium, potassium, calcium and glucose.

Exclusion Criteria:

- The patient came to the outpatient department.

- The patient did not received blood sampling at emergency room.

- The seizure occurred after admission.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Taipei Medical University-WanFang Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University WanFang Hospital

Country where clinical trial is conducted

Taiwan, 

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