UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000050280 |
|---|---|
| Receipt number | R000057253 |
| Scientific Title | Prospective multicenter study of image-guided implantation of central venous access port |
| Date of disclosure of the study information | 2023/04/22 |
| Last modified on | 2023/08/11 19:12:41 |
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Basic information
Public title
Prospective multicenter study of image-guided implantation of central venous access port
Acronym
Prospective multicenter study of central venous access port
Scientific Title
Prospective multicenter study of image-guided implantation of central venous access port
Scientific Title:Acronym
Prospective multicenter study of central venous access port
Region
| Japan |
Condition
Condition
All diseases
Classification by specialty
| Radiology |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
To prospectively evaluate image-guided implantation of central venous access port
Basic objectives2
Others
Basic objectives -Others
feasibility and safety
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Success rate of image-guided implantation of central venous access port
Key secondary outcomes
Safety
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
1) Implantation of central venous access port via following veins: internal jugular vein, subclavian (axillary) vein, brachial vein, basilic vein, cephalic vein
2) Image-guided implantation (i.e., real time ultrasound guidance and fluoroscopy using venography guidance)
3) Initial implantation
4) Observable more than 30 days
Key exclusion criteria
1) Patient has active inflammation.
2) Patient with planned indwelling vein with obvious thrombus
3) Patient with planned indwelling vein with obvious obstruction
4) Not eligible determined by the responding physician.
Target sample size
4000
Research contact person
Name of lead principal investigator
| 1st name | Toshihiro |
| Middle name | |
| Last name | IGUCHI |
Organization
Okayama University
Division name
Faculty of Health Sciences
Zip code
7008558
Address
2-5-1 Shikata-cho, Kita-ku, Okayama
TEL
+81-86-235-7313
iguchi@s.okayama-u.ac.jp
Public contact
Name of contact person
| 1st name | Toshihiro |
| Middle name | |
| Last name | IGUCHI |
Organization
Okayama University
Division name
Faculty of Health Sciences
Zip code
7008558
Address
2-5-1 Shikata-cho, Kita-ku, Okayama
TEL
+81-86-235-7313
Homepage URL
iguchi@s.okayama-u.ac.jp
Sponsor or person
Institute
Okayama University
Institute
Department
Personal name
Funding Source
Organization
Other
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
Okayama University Graduate School of Medicine, Density and Pharmaceutical Sciences and Okayama University Hospital, Ethics Committee
Address
2-5-1 Shikata-cho, Kita-ku, Okayama
Tel
086-235-6503
mae6605@adm.okayama-u.ac.jp
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
| 2023 | Year | 04 | Month | 22 | 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
| 2023 | Year | 01 | Month | 01 | Day |
Date of IRB
| 2023 | Year | 04 | Month | 28 | Day |
Anticipated trial start date
| 2023 | Year | 06 | Month | 01 | Day |
Last follow-up date
| 2026 | Year | 04 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
None
Management information
Registered date
| 2023 | Year | 02 | Month | 09 | Day |
Last modified on
| 2023 | Year | 08 | Month | 11 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000057253
