- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02394847
Does Repetitive Electroconvulsive Therapies Affect Propofol Induction Dose ?
March 17, 2015 updated by: CIGDEM YILDIRIM GUCLU, Ankara University
Does Repetitive Electroconvulsive Therapies Affect Propofol Induction Dose?
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
10
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients required electroconvulsive therapy for the physiatric disease
Exclusion Criteria:
- Patients refusal
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: propofol
dose of propofol according to the number of therapies
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
dose of propofol
Time Frame: 10 seconds
|
10 seconds
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
duration of seizure
Time Frame: 10 seconds
|
10 seconds
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2012
Primary Completion (Actual)
December 1, 2012
Study Completion (Actual)
December 1, 2012
Study Registration Dates
First Submitted
March 8, 2015
First Submitted That Met QC Criteria
March 17, 2015
First Posted (Estimate)
March 20, 2015
Study Record Updates
Last Update Posted (Estimate)
March 20, 2015
Last Update Submitted That Met QC Criteria
March 17, 2015
Last Verified
March 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 14835
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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