Can the Usage of Regional Block Room Save the Time of Anesthesia Team

December 22, 2011 updated by: Mahidol University

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

Status

Unknown

Conditions

Intervention / Treatment

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

Observational

Enrollment (Anticipated)

800

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Thailand
      • Bangkok, Thailand, 10700
        • Recruiting
        • Faculty of Medicine Siriraj Hospital, Mahidol University
        • Contact:

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

1 month and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

elective orthopedic surgical patients that require for anesthesia

Description

Inclusion Criteria:

  • elective orthopedic surgical patients that require for anesthesia ( start 9AM-4PM)

Exclusion Criteria:

  • surgery under local infiltration

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
RA in block room
Performing regional anesthesia in the block room
Procedure: regional anesthesia
regional anesthesia procedure
Other Names:
  • peripheral nerve block
  • neuraxial block
RA inside OR
Performing regional anesthesia inside the main orthopedic operating room
Procedure: regional anesthesia
regional anesthesia procedure
Other Names:
  • peripheral nerve block
  • neuraxial block

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

This is where you will find people and organizations involved with this study.

Sponsor

Mahidol University

Investigators

  • Principal Investigator: Suwimon Tangwiwat, M.D, Mahidol university

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

October 1, 2011

Primary Completion (Anticipated)

May 1, 2012

Study Completion (Anticipated)

July 1, 2012

Study Registration Dates

First Submitted

December 7, 2011

First Submitted That Met QC Criteria

December 22, 2011

First Posted (Estimate)

December 26, 2011

Study Record Updates

Last Update Posted (Estimate)

December 26, 2011

Last Update Submitted That Met QC Criteria

December 22, 2011

Last Verified

December 1, 2011

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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