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Trial of Argon Plasma Coagulation Versus APC and APC and Hemospray in the Treatment of Radiation Proctitis

Randomized Trial of Argon Plasma Coagulation Versus Argon Plasma Coagulation and Hemospray in the Therapy of Radiation Proctitis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02233933
Enrollment
20
Registered
2014-09-09
Start date
2014-09-30
Completion date
2015-12-31
Last updated
2014-09-09

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

Conditions

Rectal Bleeding

Keywords

radiation proctitis, bleeding, therapy

Brief summary

Randomized trial of Argon Plasma Coagulation compared with Argon Plasma Coagulation and Hemospray in the therapy of bleeding from Radiation Proctitis

Detailed description

20 patients with Radiation Proctitis will be randomized to receive either Argon Plasma Coagulation therapy alone or therapy with APC followed by Hemospray administration ;the treatment in each arm is administered during a sigmoidoscopic examination

Interventions

hemospray is used after argon coagulation to stop bleeding

Sponsors

British Columbia Cancer Agency
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* bleeding from radiation proctitis

Exclusion criteria

* pregnancy bleeding diathesis

Design outcomes

Primary

MeasureTime frameDescription
cessation of rectal bleeding12 monthstreatment of one group of patients with Radiation Proctitis with Argon Plasma Coagulator ( APC) and a second group will be treated with APC and Hemospray

Secondary

MeasureTime frame
number of treatments required to achieve cessation of rectal bleeding12 months

Countries

Canada

Contacts

Primary ContactAlan A Weiss, MD
aweiss@bccancer.bc.ca7789979332

Outcome results

None listed

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