UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000061972 |
|---|---|
| Receipt number | R000070897 |
| Scientific Title | An Observational Study of Side-to-Side Differences in the Onset Time of Neuromuscular Blockade in Hemodialysis Patients |
| Date of disclosure of the study information | 2026/06/19 |
| Last modified on | 2026/06/19 11:10:16 |
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Basic information
Public title
An Observational Study of Side-to-Side Differences in the Onset Time of Neuromuscular Blockade in Hemodialysis Patients
Acronym
Study of Side-to-Side Differences in Neuromuscular Blockade in Hemodialysis Patients
Scientific Title
An Observational Study of Side-to-Side Differences in the Onset Time of Neuromuscular Blockade in Hemodialysis Patients
Scientific Title:Acronym
Study of Side-to-Side Differences in Neuromuscular Blockade in Hemodialysis Patients
Region
| Japan |
Condition
Condition
Hemodialysis patients
Classification by specialty
| Anesthesiology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The objective of this study is to determine the difference in the onset time of neuromuscular blockade between the left and right upper limbs in hemodialysis patients.
Basic objectives2
Pharmacokinetics
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Onset time of neuromuscular blockade in the left and right upper limbs of hemodialysis patients.
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
| 18 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
The study will include patients undergoing maintenance hemodialysis who are scheduled for elective surgery under general anesthesia. The control group will include non-hemodialysis patients with an ASA Physical Status of I or II who are scheduled for elective surgery under general anesthesia and do not have conditions that may affect the onset of neuromuscular blockade, including neuromuscular disorders, peripheral neuropathy, or impaired upper-limb perfusion.
Key exclusion criteria
Patients who do not provide informed consent to participate in the study
Patients younger than 18 years of age
Patients with neuromuscular disorders
Target sample size
40
Research contact person
Name of lead principal investigator
| 1st name | Shinnosuke |
| Middle name | |
| Last name | Takmori |
Organization
Fukuoka City Hospital
Division name
Department of Anesthesiology
Zip code
812-0046
Address
13-1 Yoshizukahonmachi, Hakata-ku, Fukuoka, Japan
TEL
0926321111
takamori.shinnosuke.628@m.kyushu-u.ac.jp
Public contact
Name of contact person
| 1st name | Shnnouske |
| Middle name | |
| Last name | Takamori |
Organization
Fukuoka City Hospital
Division name
Department of Anesthesiology
Zip code
812-0046
Address
13-1 Yoshizukahonmachi, Hakata-ku, Fukuoka, Japan
TEL
0926321111
Homepage URL
takamori.shinnosuke.628@m.kyushu-u.ac.jp
Sponsor or person
Institute
Fukuoka City Hospital
Institute
Department
Personal name
Funding Source
Organization
Fukuoka City Hospital
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Fukuoka City Hospital
Address
13-1 Yoshizukahonmachi, Hakata-ku, Fukuoka, Japan
Tel
0926321111
takamori.shinnosuke.628@m.kyushu-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
| 2026 | Year | 06 | Month | 19 | 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
Open public recruiting
Date of protocol fixation
| 2026 | Year | 06 | Month | 15 | Day |
Date of IRB
| 2026 | Year | 06 | Month | 15 | Day |
Anticipated trial start date
| 2026 | Year | 06 | Month | 16 | Day |
Last follow-up date
| 2028 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Fukuoka City Hospital
Management information
Registered date
| 2026 | Year | 06 | Month | 19 | Day |
Last modified on
| 2026 | Year | 06 | Month | 19 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000070897
