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Status unknownNCT02233933Updated Sep 9, 2014

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

An interventional study of Hemospray in Rectal Bleeding, sponsored by British Columbia Cancer Agency. Status unknown at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-09-09.

Sponsored by British Columbia Cancer Agency · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2014), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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

Read the 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

02

Conditions studied

  • Rectal Bleeding

Keywords

  • radiation proctitis
  • bleeding
  • therapy
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In context

Gastrointestinal Hemorrhage

343 studies on the registry are indexed under Gastrointestinal Hemorrhage; 80 are open to participants now.

This study's planned enrollment of 20 is below the median of 86 across 214 interventional studies indexed under Gastrointestinal Hemorrhage.

Browse Gastrointestinal Hemorrhage studies →

Lead sponsor

British Columbia Cancer Agency is the lead sponsor of 152 studies on the registry; 33 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

  • bleeding from radiation proctitis

Exclusion criteria

Exclusion Criteria:

  • pregnancy bleeding diathesis
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Active comparator
    argon plasma coagulation

    argon plasma coagulation of radiation proctitis

    Other: Hemospray

  • Experimental
    argon plasma coagulator and hemospray

    treatment of radiation proctitis with argon plasma coagulator followed by application of hemospray

    Other: Hemospray

Interventions

  • OtherHemospray

    hemospray is used after argon coagulation to stop bleeding

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What researchers measure

Primary outcomes

  1. cessation of rectal bleeding

    treatment of one group of patients with Radiation Proctitis with Argon Plasma Coagulator ( APC) and a second group will be treated with APC and Hemospray

    Time frame: 12 months

Secondary outcomes

  1. number of treatments required to achieve cessation of rectal bleeding

    Time frame: 12 months

07

Study locations

1 site
  • British Columbia Cancer Clinic
    Vancouver, British Columbia, Canada
    • Alan A Weiss, MD · Contact · aweiss@bccancer.bc.ca · 778 9979332
    • Alan A Weiss, MD · Principal investigator
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02233933
Responsible party
Alan Weiss (Principal Investgator, British Columbia Cancer Agency) — Principal investigator
First posted
Sep 9, 2014
Start date
Sep 2014
Primary completion
Dec 2015 (estimated)
Completion
Dec 2015 (estimated)
Last update
Sep 9, 2014

Study contacts

Alan A Weiss, MD
Contact
aweiss@bccancer.bc.ca
7789979332
Alan A Weiss, MD
principal investigator · BCCA

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2014. You cannot join it, but the record below documents what was studied.

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