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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02394847
Other study ID # 14835
Secondary ID
Status Completed
Phase N/A
First received March 8, 2015
Last updated March 17, 2015
Start date January 2012
Est. completion date December 2012

Study information

Verified date March 2015
Source Ankara University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ministry of Health
Study type Interventional

Clinical Trial Summary

Electroconvulsive therapy has been used for many years for different types of physiatric diseases. General anesthesia is used during the procedure. Different anesthesiologists use different regimens. The duration of seizure is important in this procedure. The investigators evaluated the relationship between the dose of propofol and the number of electroconvulsive therapy and duration of the seizure.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients required electroconvulsive therapy for the physiatric disease

Exclusion Criteria:

- Patients refusal

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Screening


Related Conditions & MeSH terms


Intervention

Drug:
propofol


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ankara University

Outcome

Type Measure Description Time frame Safety issue
Primary dose of propofol 10 seconds No
Secondary duration of seizure 10 seconds No
See also
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Completed NCT05408000 - Comparision of Motor Seizure Duration of Ketofol and Propofol for Electroconvulsive Therapy N/A
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