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Seed Movement in Prostate Brachytherapy Implants: Clinical Measurement and Dosimetric Consequences

Seed Movement in Prostate Brachytherapy Implants: Clinical Measurement and Dosimetric Consequences

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01355185
Enrollment
20
Registered
2011-05-18
Start date
2011-08-31
Completion date
2015-06-30
Last updated
2014-10-03

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

Conditions

Prostate Cancer

Keywords

Seed movement, implants, prostate brachytherapy, localized

Brief summary

There are substantial uncertainties with contemporary seed placement techniques in prostate brachytherapy, particularly with the impact of seed movement after an implant due to edema and migration of seeds in the prostate and peri-prostatic tissues. This study will accrue 20 patients undergoing prostate brachytherapy implants and perform serial CT and MRI scans at specified intervals (pre-operatively, day 0, day 3, day 10 and day 28) to characterize these phenomena.

Detailed description

Prostate brachytherapy is an effective treatment option for men with localized prostate cancer with excellent cure rates and a favorable toxicity profile. Having a more detailed understanding of seed movement after an implant will provide clinicians with details about the clinical impact of these phenomena on implants and provide the detailed understanding of these phenomena that are necessary for more sophisticated brachytherapy implants that are envisioned in the future.

Interventions

None listed

Sponsors

Canadian Association of Radiation Oncology
CollaboratorINDUSTRY
Sanofi
CollaboratorINDUSTRY
AHS Cancer Control Alberta
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* treated with prostate brachytherapy * low risk or intermediate risk prostate cancer * ambulatory * stable medical condition * 18 years of age or older * capable of informed consent

Exclusion criteria

* no use of any hormonal therapy * unable to have MRI scans (ie. presence of metallic foreign object, aneurysm clip, cardiac pacemaker, internal wires, implanted pump, implanted cardiac device, claustrophobia, etc.

Countries

Canada

Contacts

Primary ContactNawaid Usmani, MD, FRCPC
Nawaid.Usmani@albertahealthservices.ca780-432-8518
Backup ContactRonald Sloboda, PhD
Ron.Sloboda@albertahealthservices.ca780-432-8719

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026