- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01499589
Can the Usage of Regional Block Room Save the Time of Anesthesia Team
Can the Usage of Regional Block Room Save the Time of Anesthesia Team in the Main Orthopedic Operating Room?
Study of time usage of anesthesia team inside the main operating room compares between 2 groups of
- Performing regional anesthesia inside the operating room
- Performing regional anesthesia in the block room
Study purpose: How much will the investigators save time in the main operating room if we perform the regional anesthesia in the block room?
Study Overview
Detailed Description
Anesthesia-controlled time means anesthesia pre-procedure time plus anesthesia post-procedure time.
We also compares the anesthesia-controlled time in 3 groups of
- general anesthesia
- regional anesthesia
- general anesthesia combined with regional anesthesia
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
-
Bangkok, Thailand, 10700
- Recruiting
- Faculty of Medicine Siriraj Hospital, Mahidol University
-
Contact:
- Suwimon Tangwiwat, M.D
- Phone Number: (66)81-645-6167
- Email: stangwiwat@yahoo.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- elective orthopedic surgical patients that require for anesthesia ( start 9AM-4PM)
Exclusion Criteria:
- surgery under local infiltration
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
RA in block room
Performing regional anesthesia in the block room
|
regional anesthesia procedure
Other Names:
|
|
RA inside OR
Performing regional anesthesia inside the main orthopedic operating room
|
regional anesthesia procedure
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
anesthesia-controlled time
Time Frame: 3 months
|
anesthesia-controlled time = anesthesia pre-procedure time + anesthesia post-procedure time
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
turnover time
Time Frame: 3 months
|
turnover time = time new patient-in minus previous patient-out
|
3 months
|
|
number of elective cases after 4PM
Time Frame: 3 months
|
number of the elective cases that will be running after 4 PM
|
3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Suwimon Tangwiwat, M.D, Mahidol University
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Si562/2011
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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