UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000057391 |
|---|---|
| Receipt number | R000065575 |
| Scientific Title | Comparison of general anesthesia versus regional anesthesia utilizing block room on the carbon footprint in orthopedic surgery |
| Date of disclosure of the study information | 2025/03/25 |
| Last modified on | 2025/03/25 10:44:35 |
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Basic information
Public title
Comparison of general anesthesia versus regional anesthesia utilizing block room on the carbon footprint in orthopedic surgery
Acronym
Genereal vs. Regional anesthesia on carbon footprint in orthopedic surgery
Scientific Title
Comparison of general anesthesia versus regional anesthesia utilizing block room on the carbon footprint in orthopedic surgery
Scientific Title:Acronym
Genereal vs. Regional anesthesia on carbon footprint in orthopedic surgery
Region
| Asia(except Japan) |
Condition
Condition
Patients who underwent extremity surgery (hand, shoulder, knee, ankle, hip, etc.) that can be performed under general or regional anesthesia
Classification by specialty
| Surgery in general | Orthopedics |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
This study compares and analyzes the carbon footprints of general anesthesia and regional anesthesia using a regional anesthesia room in orthopedic surgery, and suggests directions for eco-friendly medical practices.
Basic objectives2
Others
Basic objectives -Others
This study compares and analyzes the carbon footprints of general anesthesia and regional anesthesia using a regional anesthesia room in orthopedic surgery, and suggests directions for eco-friendly medical practices.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Carbon Footprint (gCO2e), the amount of carbon dioxide emitted, is calculated and compared to the IPCC GWP 100a (kg CO2 eq) standard by considering the amount of carbon dioxide emitted, such as drugs or devices used.
Key secondary outcomes
Base
Study type
Observational
Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
Purpose of intervention
Type of intervention
Interventions/Control_1
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
patients who underwent orthopedic extremity surgery (hand, shoulder, knee, ankle, hip, etc.) that can be performed under general or regional anesthesia.
Key exclusion criteria
ASA class 5
Target sample size
400
Research contact person
Name of lead principal investigator
| 1st name | Seok Kyeong |
| Middle name | |
| Last name | Oh |
Organization
Korea University Guro Hospital
Division name
Seoul
Zip code
08308
Address
148, Gurodong-ro, Guro-gu, Seoul
TEL
82-2-2626-3234
nanprayboy@korea.ac.kr
Public contact
Name of contact person
| 1st name | Seok Kyeong |
| Middle name | |
| Last name | Oh |
Organization
Korea University Guro Hospital
Division name
Seoul
Zip code
08308
Address
148, Gurodong-ro, Guro-gu, Seoul
TEL
82-2-2626-3234
Homepage URL
nanprayboy@korea.ac.kr
Sponsor or person
Institute
Department of Anesthesiology and Pain Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Institute
Department
Personal name
Funding Source
Organization
Korea University College of Medicine, Seoul, Republic of Korea.
Organization
Division
Category of Funding Organization
Outside Japan
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Korea University Guro Hospital
Address
148, Gurodong-ro, Guro-gu, Seoul 08308, Korea
Tel
82-2-2626-1635
eirbadmin@kumc.or.kr
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2025 | Year | 03 | Month | 25 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Enrolling by invitation
Date of protocol fixation
| 2025 | Year | 01 | Month | 23 | Day |
Date of IRB
| 2025 | Year | 01 | Month | 23 | Day |
Anticipated trial start date
| 2025 | Year | 01 | Month | 23 | Day |
Last follow-up date
| 2025 | Year | 03 | Month | 21 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
This study will analyze the anesthesia records among the collected medical records, and anonymize and save the data during the process of transferring it to Excel.
- Data collection method: Anesthesia record review
- Anonymization method: Use data from which personal identification information has been completely removed by a third party and a separate identification code has been assigned.
Management information
Registered date
| 2025 | Year | 03 | Month | 25 | Day |
Last modified on
| 2025 | Year | 03 | Month | 25 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065575
