Budesonide Foam Versus Placebo for Prevention of Acute Radiation Proctitis (NCT00828230) | Clinical Trial Compass
TerminatedPhase 2
Budesonide Foam Versus Placebo for Prevention of Acute Radiation Proctitis
Stopped: Study was prematurely stopped due to slow recruitment after 17 of 32 anticipated patients were recruited.
Germany17 participantsStarted 2008-09
Plain-language summary
To proof the superiority of an 8-week rectal treatment with once-daily 2 mg budesonide versus placebo for the prevention of acute radiation proctitis, and to evaluate the occurrence of chronic radiation proctitis 1 year after start of radiation therapy.
Who can participate
Age range18 Years
SexMALE
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Inclusion Criteria:
* Signed informed consent,
* Men aged at least 18 years,
* Patients with ECOG performance status \<= 2 or Karnofsky Performance Status Scale \>= 70%,
* Estimated life expectancy more than 3 years,
* Diagnosis of prostate carcinoma,
* Indication for local RT in patients with prostatic cancer.
Exclusion Criteria:
* Crohn's disease, indeterminate colitis, ulcerative colitis, microscopic colitis (i.e., collagenous colitis and lymphocytic colitis),
* Severe or symptomatic ischaemic colitis at baseline,
* Grade III internal haemorrhoids at baseline,
* High risk patients needing extended radiation therapy,
* Acute EORTC/RTOG lower GI toxicity score of \>=1 at baseline,
* Bacterial, amoebic, fungal, or viral infections of the gut,
* Tuberculosis, hypertension, infection, diabetes mellitus (included familiarly predisposition), active peptic ulcer, osteoporosis, glaucoma, or cataract, if careful medical monitoring is not ensured,
* Portal hypertension or liver cirrhosis,
* Abnormal hepatic function (ALT, AST or AP \> 2.5 x ULN),
* Known intolerance/hypersensitivity/resistance to study drug or drugs of similar chemical structure or pharmacological profile, or to any of the other constituents of the study drug,
* Participation in another clinical trial within the last 30 days, simultaneous participation in another clinical trial, or previous participation in this trial
What they're measuring
1
Proportion of patients developing radiation proctitis during treatment or need rescue medication