NCT06452212

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
23

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jul 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 5, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 11, 2024

Completed
29 days until next milestone

Study Start

First participant enrolled

July 10, 2024

Completed
19 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 29, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 29, 2024

Completed
Last Updated

November 21, 2024

Status Verified

November 1, 2024

Enrollment Period

19 days

First QC Date

June 5, 2024

Last Update Submit

November 19, 2024

Conditions

Keywords

mHSPCUrological cancers

Outcome Measures

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.

    Up to 7 days

Study Arms (1)

Urologists

Health care professionals/panelist.

Other: No Intervention

Interventions

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

Urologists

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-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.

You may qualify if:

  • 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.

You may not qualify if:

  • Urologist in private practice.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

KR82001

Seoul, South Korea

Location

MeSH Terms

Conditions

Urologic Neoplasms

Condition Hierarchy (Ancestors)

Urogenital NeoplasmsNeoplasms by SiteNeoplasmsFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesUrologic Diseases

Study Officials

  • Medical Director

    Astellas Pharma Korea, Inc.

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 5, 2024

First Posted

June 11, 2024

Study Start

July 10, 2024

Primary Completion

July 29, 2024

Study Completion

July 29, 2024

Last Updated

November 21, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

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/.

Locations