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Hemostatic Single 8 Gy radiotherapy for Tumor bleeding Palliation

Hemostatic Single 8 Gy radiotherapy for Tumor bleeding Palliation - HemoStop Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000059654
Enrollment
100
Registered
2025-11-06
Start date
2025-02-17
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

All cancers with tumor-related bleeding

Interventions

None listed

Sponsors

National Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients scheduled to receive radiotherapy with a single 8 Gy fraction for tumor-related bleeding 2) Patients aged 20 years or older at the time of obtaining consent 3) Patients who have provided oral informed consent

Exclusion criteria

Exclusion criteria: 1) Patients for whom follow-up is expected to be difficult (e.g., those living far from the hospital or with a performance status of 4 or higher)

Design outcomes

Primary

MeasureTime frame
Hemostatic response rate

Secondary

MeasureTime frame
rebleeding rate, time to first rebleeding, overall survival

Countries

Japan

Contacts

Public ContactKenji Makita

National Cancer Center Hospital East Department of Radiation Oncology

kemaki3@east.ncc.go.jp0471331111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026