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Name:
UMIN ID:

Recruitment status Enrolling by invitation
Unique ID issued by UMIN UMIN000039892
Receipt No. R000045496
Scientific Title Clinical meaning of serum zinc deficiency in patients with inflammatory bowel diseases
Date of disclosure of the study information 2020/05/11
Last modified on 2020/05/23

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Basic information
Public title Evaluation of time-course changes of clinical symptoms in patients with inflammatory bowel diseases with serum zinc deficiency
Acronym Clinical characteristics in IBD patients with serum zinc deficiency
Scientific Title Clinical meaning of serum zinc deficiency in patients with inflammatory bowel diseases
Scientific Title:Acronym Clinical meaning of serum zinc deficiency in IBD patients
Region
Japan

Condition
Condition Ulcerative colitis and Crohn's disease
Classification by specialty
Medicine in general Gastroenterology
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 Evaluation of clinical manifestation in IBD patients with serum zinc deficiency, as well as improvement of clinical activity and manifestation after zinc replacement therapy
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Changes of Visual Analogue Score (VAS) of fatigue after the zinc replacement therapy
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 with ulcetative colitis or Crohn's disease
Key exclusion criteria 1. Patients without informed consent
2. Inappropriate patients for this study determined by doctors
Target sample size 60

Research contact person
Name of lead principal investigator
1st name Shingo
Middle name
Last name Kato
Organization Saitama Medical Center, Saitama Medical University
Division name Department of Gastroenterology and Hepatology
Zip code 350-8550
Address 1981 Kamoda, Kawagoe City, Saitama 3508550, Japan
TEL 049-228-3564
Email skato@saitama-med.ac.jp

Public contact
Name of contact person
1st name Shingo
Middle name kato
Last name kato
Organization Saitama Medical Center, Saitama Medical University
Division name Department of Gastroenterology and Hepatology
Zip code 350-8550
Address 1981 Kamoda, Kawagoe City, Saitama 3508550, Japan
TEL 049-228-3564
Homepage URL
Email skato@saitama-med.ac.jp

Sponsor
Institute Saitama Medical Center, Saitama Medical University
Institute
Department

Funding Source
Organization Saitama Medical Center, Saitama Medical University
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 IRB of Saitama Medical Center
Address 1981 Kamoda, Kawagoe City, Saitama 3508550, Japan
Tel 049-228-3902
Email smcrinri@saitama-med.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
2020 Year 05 Month 11 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
2020 Year 05 Month 07 Day
Date of IRB
2020 Year 05 Month 14 Day
Anticipated trial start date
2020 Year 05 Month 15 Day
Last follow-up date
2023 Year 03 Month 31 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information We will evaluate the VAS score of fatigue, abnormal taste, "Jikakushojo-Shirabe" and Clinical Activities, such as CDAI and partial Mayo score before and after the zinc replacement therapy in IBD patients in our hospital.

Management information
Registered date
2020 Year 03 Month 20 Day
Last modified on
2020 Year 05 Month 23 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045496

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


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