Radiation Injuries Clinical Trial
Official title:
A Randomized Prospective Study of Endoscopy Bipolar Eletrocoagulation and Argon Plasma Coagulation of Chronic Rectal Bleeding From Radiation Telangiectasias
Aim:
To compare the efficacy, safety and number of sessions of bipolar eletrocoagulation (BEC)
and argon plasma coagulation (APC) in the management of the bleeding telangiectasias from
chronic radiation coloproctopathy (CRCP).
Methods:
Thirty patients with active bleeding from telangiectasias were enrolled in two groups (15
BEC and 15 APC) and classified according of Saunders score. BEC settings were 50 W and APC
settings were 40 W and 1.0 l/min. Colonoscopy was the first exam to rule out synchronous
lesions and follow-up was performed with sigmoidoscopies. Clinical cure was defined as
cessation of bleeding and endoscopic cure was determined by absence of telangiectasias.
Failure was defined whenever more than 7 sessions or other therapy was necessary.
Thirty patients with active and chronic hematochezia from radiation telangiectasias were
randomized in two groups :
- fifteen patients in group 1- bipolar eletrocoagulation (BE) and
- fifteen in group 2 - argon plasma coagulation(APC). For inclusion in the study, all
patients were required to have active (at least one episode last week) and chronic
(persist or appear 6 months after the conclusion of radiotherapy) rectal bleeding.
Between May 2005 and April 2008, patients were treated and followed at the Endoscopy
Unit in the São Paulo Hospital (UNIFESP).
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04059809 -
Photobiomodulation for Breast Cancer Radiodermatitis
|
Phase 2/Phase 3 | |
Completed |
NCT02985164 -
Radiation Exposure During Endoscopic Retrograde Cholangiopancreatography
|
Phase 3 | |
Recruiting |
NCT04152681 -
Effect and Safety of Apatinib on Radiation-Induced Brain Injury
|
Phase 2 | |
Recruiting |
NCT04818099 -
Vortioxetine in the Treatment of Depression Associated With Head and Neck Cancers Undergoing Radiotherapy
|
Phase 3 | |
Completed |
NCT03667859 -
Vaginal Elasticity Assessment Before and After Brachytherapy/Pelvic Radiation
|
||
Terminated |
NCT03660618 -
LSFG-SKIN, Laser Speckle Flowgraphy
|
N/A | |
Completed |
NCT00001523 -
Structure and Functional Status of Parotid Glands Exposed to Therapeutic Irradiation
|
N/A | |
Recruiting |
NCT03907371 -
The Effect of Donepezil in Radiotherapy-related Cognitive Impairment.
|
Phase 2 | |
Not yet recruiting |
NCT05063773 -
Novel Wireless Mixed Reality Headset for Image Guidance in Cardiac Catheterization Laboratory
|
N/A | |
Completed |
NCT00001437 -
Trial of Pentoxifylline in Patients With Functional Disability Caused by Radiation-Induced Advanced Regional Fibrosis
|
Phase 2 | |
Recruiting |
NCT06325982 -
Clinical Observation of Drug Retention Enema in Preventing Acute Radiation-induced Rectal Injury
|
N/A | |
Recruiting |
NCT03208413 -
The Therapeutic Effect of Thalidomide in RI
|
Phase 2 | |
Completed |
NCT02972736 -
RadiatiOn Dose Among Different EndOvascular Procedures: the RODEO Study
|
||
Completed |
NCT02104271 -
Comparison Between Two Different Parameters of Argon Plasma Coagulation in the Treatment of Chronic Radiation Proctitis: Historical Control Trial.
|
Phase 2 | |
Terminated |
NCT00134628 -
Study to Determine if Hyperbaric Oxygen Therapy is Helpful for Treating Radiation Tissue Injuries
|
Phase 3 | |
Completed |
NCT03961217 -
Return to Work Among Cancer Survivors With Treatment-induced Survivorship Syndromes
|