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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00207961
Other study ID # DMR-93-43
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated December 8, 2005
Start date October 2003
Est. completion date October 2004

Study information

Verified date September 2005
Source China Medical University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

Using patients receiving spinal anesthesia as a model to evaluate the treshold value of cerebral oximeter to detect the symptoms of cerebral ischemia


Description:

56 patients has been recruited for the analysis of relationship between the symptoms of cerebral ischemia and the value of cerebral oximeter. All patients were recieved spinal anesthesia for the procedure of Ceserean section.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date October 2004
Est. primary completion date
Accepts healthy volunteers
Gender Female
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria: patients who are going to undergo Cesarean section under spinal anesthesia

Exclusion Criteria: conditons contraindicated for regional anesthesia

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Longitudinal


Locations

Country Name City State
Taiwan Anesthetic Department Taichung

Sponsors (1)

Lead Sponsor Collaborator
China Medical University Hospital

Country where clinical trial is conducted

Taiwan, 

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