UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000054147
Receipt number R000061831
Scientific Title Anion gap method for lithium poisoning identification: A single-center retrospective observational study
Date of disclosure of the study information 2024/04/14
Last modified on 2024/04/14 15:44:57

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Basic information

Public title

Anion gap method for lithium poisoning identification: A single-center retrospective observational study

Acronym

Anion gap method for lithium poisoning identification

Scientific Title

Anion gap method for lithium poisoning identification: A single-center retrospective observational study

Scientific Title:Acronym

Anion gap method for lithium poisoning identification

Region

Japan


Condition

Condition

Lithium poisoning

Classification by specialty

Psychiatry Laboratory medicine Emergency medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study aimed to evaluate the feasibility of utilizing the anion gap as a diagnostic tool for detecting lithium intoxication. Additionally, we would examine the effectiveness of correcting the anion gap for albumin and lactate values compared to conventional anion gap calculation methods.

Basic objectives2

Others

Basic objectives -Others

Investigation of diagnostic accuracy

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Diagnostic accuracy of the anion gap for lithium poisoning

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

Patients whose lithium blood levels were assessed at the emergency department and admitted to the Emergency Medical Center of Niigata University Medical and Dental Hospital between January 2014 and December 2023.

Key exclusion criteria

In case of missing data

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Hiroyuki
Middle name
Last name Honda

Organization

Niigata University Medical and Dental Hospital

Division name

Department of Critical Care Medicine

Zip code

951-8510

Address

754, Ichibancho, Asahimachidori, Chuo-ku, Niigata-shi, Niigata, Japan

TEL

025-223-6161

Email

h.honda0914@gmail.com


Public contact

Name of contact person

1st name Hiroyuki
Middle name
Last name Honda

Organization

Niigata University Medical and Dental Hospital

Division name

Department of Critical Care Medicine

Zip code

951-8510

Address

754, Ichibancho, Asahimachidori, Chuo-ku, Niigata-shi, Niigata, Japan

TEL

025-223-6161

Homepage URL


Email

h.honda0914@gmail.com


Sponsor or person

Institute

Niigata University Medical and Dental Hospital

Institute

Department

Personal name

Hiroyuki Honda


Funding Source

Organization

Self-funding

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

Ethics Committee of Niigata University

Address

757, Ichibancho, Asahimachidori, Chuo-ku, Niigata-shi, Niigata, Japan

Tel

025-227-2625

Email

ethics@adm.niigata-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

2024 Year 04 Month 14 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

18

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

No longer recruiting

Date of protocol fixation

2023 Year 05 Month 07 Day

Date of IRB

2023 Year 06 Month 29 Day

Anticipated trial start date

2023 Year 05 Month 07 Day

Last follow-up date

2026 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Clinical information will be analyzed based on data obtained from medical records. It is important to note that the information used in this study have been previously collected during general practice and will not be newly obtained.


Management information

Registered date

2024 Year 04 Month 14 Day

Last modified on

2024 Year 04 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000061831


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name