UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000052286
Receipt number R000059688
Scientific Title Frequency of Hypertension in Childhood Cancer Survivors: a systematic review and meta-analysis
Date of disclosure of the study information 2023/10/01
Last modified on 2023/09/22 23:53:22

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Basic information

Public title

Frequency of Hypertension in Childhood Cancer Survivors: a systematic review and meta-analysis

Acronym

Frequency of Hypertension in Childhood Cancer Survivors: a systematic review and meta-analysis

Scientific Title

Frequency of Hypertension in Childhood Cancer Survivors: a systematic review and meta-analysis

Scientific Title:Acronym

Frequency of Hypertension in Childhood Cancer Survivors: a systematic review and meta-analysis

Region

Japan


Condition

Condition

Childhood Cancers

Classification by specialty

Medicine in general Cardiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

A Systematic Review and Meta-Analysis of the Incidence of Hypertension in Childhood Cancer Survivors

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The primary outcome: The prevalence of hypertension will be pooled using random effects model meta-analysis.

Key secondary outcomes



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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

(1) Studies are case-control studies, cohort studies, or randomized clinical trials.
(2) Studies are of clinically diagnosed pediatric malignancies and include survivor patients.
(3) Studies are reporting on the complications of hypertension.

Key exclusion criteria

(1)A systematic review or meta-analysis article.
(2)Case reports or case series with fewer than 5 cases.
(3)Exclude republished research literature unless it contains new findings related to hypertension.
(4)Studies published in languages other than English.

Target sample size



Research contact person

Name of lead principal investigator

1st name Shintaro
Middle name
Last name Minegishi

Organization

Yokohama City University Graduate School of Medicine

Division name

Department of Cardiology

Zip code

236-0004

Address

3-9, Kanazawa, Fukuura, Yokohama

TEL

045-787-2635

Email

minegishi.shi.fb@yokohama-cu.ac.jp


Public contact

Name of contact person

1st name Shintaro
Middle name
Last name Minegishi

Organization

Yokohama City University Graduate School of Medicine

Division name

Department of Cardiology

Zip code

236-0004

Address

3-9, Kanazawa, Fukuura, Yokohama

TEL

045-787-2635

Homepage URL


Email

minegishi.shi.fb@yokohama-cu.ac.jp


Sponsor or person

Institute

Yokohama City University Graduate School of Medicine

Institute

Department

Personal name



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

Yokohama City University Graduate School of Medicine

Address

3-9, Kanazawa, Fukuura, Yokohama

Tel

045-787-2635

Email

minegishi.shi.fb@yokohama-cu.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 10 Month 01 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

Preinitiation

Date of protocol fixation

2023 Year 09 Month 22 Day

Date of IRB


Anticipated trial start date

2023 Year 09 Month 22 Day

Last follow-up date

2024 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Candidate papers will be searched in October 2023 using PubMed, Cochrane, EMBASE, and Web of Science Core Collection. Hand searches will be conducted by two persons.

Participants: Childhood Cancer Survivors
Intervention: Treatment of malignant tumors
Comparison: None
Outcome: Development of hypertension

Two investigators will independently review all titles, abstracts, and full texts for eligibility. Final inclusion will be determined after resolution of any discrepancies between the two investigators.

The risk of bias for each study will be assessed using the Newcastle-Ottawa Scale for Cohort Studies.


Management information

Registered date

2023 Year 09 Month 22 Day

Last modified on

2023 Year 09 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000059688