UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000012854 |
|---|---|
| Receipt number | R000015019 |
| Scientific Title | Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height? |
| Date of disclosure of the study information | 2014/01/15 |
| Last modified on | 2014/11/20 13:01:59 |
* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments
Basic information
Public title
Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?
Acronym
Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?
Scientific Title
Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?
Scientific Title:Acronym
Can we really predict the appropriate insertion depth for a double-lumen endobronchial tube by patient height?
Region
| Japan |
Condition
Condition
lung cancer, pneumothorax
Classification by specialty
| Chest surgery | Anesthesiology |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
Our purpose is to investigate whether we can predict the appropriate insertion depth for a double-lumen endotracheal tube by patient height.
Basic objectives2
Safety
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Explanatory
Developmental phase
Not applicable
Assessment
Primary outcomes
Correlation between patient height and insertion depth for each gender
Key secondary outcomes
Correlation between patient height and insertion depth for both male and female patients
Base
Study type
Others,meta-analysis etc
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
| 18 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Patients who underwent thoracic surgery with a left double-lumen endotracheal tube
Key exclusion criteria
Patients were excluded when one-lung ventilation was not performed properly.
Target sample size
412
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | MASATO SATO |
Organization
Keiyu Hospital
Division name
Department of Anesthesiology
Zip code
Address
3-7-3 Minatomirai Nishiku Yokohama Japan
TEL
045-221-8181
keiyumasui@gmail.com
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | MASATO SATO |
Organization
Keiyu Hospital
Division name
Department of Anesthesiology
Zip code
Address
3-7-3 Minatomirai Nishiku Yokohama Japan
TEL
045-221-8181
Homepage URL
keiyumasui@gmail.com
Sponsor or person
Institute
Keiyu Hospital
Institute
Department
Personal name
Funding Source
Organization
Keiyu Hospital
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Address
Tel
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
| 2014 | Year | 01 | Month | 15 | Day |
Related information
URL releasing protocol
Publication of results
Partially published
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
Preinitiation
Date of protocol fixation
| 2014 | Year | 01 | Month | 15 | Day |
Date of IRB
Anticipated trial start date
| 2014 | Year | 01 | Month | 15 | Day |
Last follow-up date
| 2014 | Year | 11 | Month | 20 | Day |
Date of closure to data entry
| 2014 | Year | 11 | Month | 20 | Day |
Date trial data considered complete
| 2014 | Year | 11 | Month | 20 | Day |
Date analysis concluded
| 2014 | Year | 11 | Month | 20 | Day |
Other
Other related information
This retrospective study included 412 adult patients (287 men and 125 women) undergoing thoracic surgery with a left-sided double-lumen endotracheal tube.
Management information
Registered date
| 2014 | Year | 01 | Month | 15 | Day |
Last modified on
| 2014 | Year | 11 | Month | 20 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015019
