UMIN-CTR Clinical Trial

Basic information
Public title	The effect of frailty on quality of life and lower urinary symptoms after robot-assisted radical prostatectomy: A longitudinal analysis (FRARP-QL study)
Acronym	The effect of frailty on quality of life and lower urinary symptoms after robot-assisted radical prostatectomy: A longitudinal analysis (FRARP-QL study)
Scientific Title	The effect of frailty on quality of life and lower urinary symptoms after robot-assisted radical prostatectomy: A longitudinal analysis (FRARP-QL study)
Scientific Title:Acronym	The effect of frailty on quality of life and lower urinary symptoms after robot-assisted radical prostatectomy: A longitudinal analysis (FRARP-QL study)
Region	Japan

Condition
Condition	prostate cancer
Classification by specialty	Urology
Classification by malignancy	Malignancy
Genomic information	NO

Objectives
Narrative objectives1	We aimed to evaluate the effect of frailty on and health-related quality of life (HRQOL) and lower urinary symptoms (LUTS) after robot-assisted radical prostatectomy (RARP) in patients with prostate cancer (PC).
Basic objectives2	Efficacy
Basic objectives -Others
Trial characteristics_1	Exploratory
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes	The effect of frailty on HRQOL between the frail and nonfrail groups from the baseline to 12 months after RARP.
Key secondary outcomes	The effect of frailty on LUTS between the frail and nonfrail groups from the baseline to 12 months after RARP.

Base
Study type	Observational

Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
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Purpose of intervention
Type of intervention
Interventions/Control_1
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Eligibility
Age-lower limit	20 years-old <=
Age-upper limit	100 years-old >
Gender	Male
Key inclusion criteria	Patients with prostate cancer treated with robot-assisted radical prostatectomy (RARP)
Key exclusion criteria	Patients with prostate cancer treated with radiotherapy or androgen deprivation therapy, and without HRQOL evaluation for 12 months.
Target sample size	200

Research contact person
Name of lead principal investigator	1st name Shingo Middle name Hatakeyama Last name Hatakeyama
Organization	Hirosaki University Graduate School of Medicine
Division name	Urology
Zip code	036-8562
Address	Hirosaki
TEL	0172395091
Email	shingorilla2@gmail.com

Public contact
Name of contact person	1st name Shingo Middle name Hatakeyama Last name Hatakeyama
Organization	Dept. of Urology, Hirosaki University Graduate School of Medicine
Division name	Urology
Zip code	036-8562
Address	Hirosaki
TEL	0172395091
Homepage URL
Email	shingorilla2@gmail.com

Sponsor
Institute	Hirosaki University Graduate School of Medicine
Institute
Department

Funding Source
Organization	Hirosaki University Graduate School of Medicine
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	Dept. of Urology, Hirosaki University Graduate School of Medicine
Address	5 Zaifu-chou, Hirosaki
Tel	+81172395091
Email	rinri@hirosaki-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	2020 Year 05 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
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Results Delayed
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Baseline Characteristics
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Progress
Recruitment status	Enrolling by invitation
Date of protocol fixation	2017 Year 01 Month 06 Day
Date of IRB	2017 Year 01 Month 06 Day
Anticipated trial start date	2017 Year 01 Month 06 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	Evaluation of the geriatric 8 screening (G8) scores, SF-8 Health Survey (SF-8), Expanded Prostate Cancer Index Composite (EPIC), International Prostate Symptom Score (IPSS), and Overactive Bladder Symptom Score (OABSS) for 12 months.

Management information
Registered date	2020 Year 04 Month 28 Day
Last modified on	2020 Year 04 Month 29 Day

Link to view the page
URL(English)	https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045936

Research Plan
Registered date	File name

Research case data specifications
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Research case data
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