ClinicalTrials.gg
CompletedNCT06452212Updated Nov 21, 2024

Non-Interventional Study to Establish Consensus on Management of Metastatic Hormone-Sensitive Prostate Cancer Patients

An observational study in Metastatic Hormone-Sensitive Prostate Cancer, sponsored by Astellas Pharma Korea, Inc.. Completed at 1 site in Korea, Republic of. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-11-21.

Sponsored by Astellas Pharma Korea, Inc. (part of Astellas Pharma Inc) · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
23
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to establish an expert consensus recommendations on managing patients with mHSPC in South Korea, and to provide clinicians with a comprehensive guide to support their clinical decision making. There are no secondary objectives for this study.

Read the detailed description

Data collection for this study will be conducted through 2 rounds of web-based surveys of health care professionals (HCPs). A meeting with the panelists will be held as a 3rd round if a consensus for pre determined key questions is not achieved after the 2 rounds of the survey.

02

Conditions studied

  • Metastatic Hormone-Sensitive Prostate Cancer

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Keywords

  • mHSPC
  • Urological cancers
03

In context

Urologic Neoplasms

155 studies on the registry are indexed under Urologic Neoplasms; 40 are open to participants now.

This study's enrollment of 23 is below the median of 174 across 33 observational studies indexed under Urologic Neoplasms.

Browse Urologic Neoplasms studies →

Lead sponsor

Astellas Pharma Korea, Inc. is the lead sponsor of 19 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Target recruitment of 25 urologists will be recruited with an acceptable goal of 20 as panelists from university hospitals in South Korea.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Urologist from university hospitals in South Korea.
  • Has a minimum 10 years of practice experience (experience as a military or public health doctor could be considered practice experience)
  • Sees a minimum of 50 mHSPC patients in a year.
  • At least 10 publications in SCIE (Science Citation Index Expanded) journals in the past 5 years.

Exclusion criteria

Exclusion Criteria:

  • Urologist in private practice.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
23 participants (actual)
Patient registry
No

Groups and cohorts

  • Urologists

    Health care professionals/panelist.

    Other: No Intervention

Interventions

  • OtherNo Intervention

    No investigational drug will be administered to participants in this study.

06

What researchers measure

Primary outcomes

  1. Treatment plans for patients with mHSPC

    Treatment plans for patients with mHSPC within the local healthcare environment will be collected via online surveys and a consensus meeting will be held if required.

    Time frame: Up to 7 days

07

Study locations

1 site
  • KR82001
    Seoul, Korea, Republic of
08

References and documents

Individual participant data

Plan to share: No — Access to anonymized individual participant level data will not be provided for this trial. Further details on Astellas' data sharing policy can be found at https://www.clinicaltrials.astellas.com/transparency/.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jul 2024 to primary completion in Jul 2024, 0 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 5, 2024
First posted
Jun 11, 2024
StartActual
Jul 10, 2024
Primary completionActual
Jul 29, 2024
CompletionActual
Jul 29, 2024
Last update
Nov 21, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 21, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06452212
Responsible party
Sponsor
First posted
Jun 11, 2024
Start date
Jul 10, 2024
Primary completion
Jul 29, 2024
Completion
Jul 29, 2024
Last update
Nov 21, 2024

Study contacts

Medical Director
study director · Astellas Pharma Korea, Inc.

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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