WHO ICTRP trial
Evaluation of the Radioprotective Effect of Famotidine Against Radiotherapy…
ACTRN12612000101886 · Australian New Zealand Clinical Trials Registry (ANZCTR) · Not Recruiting
Key facts
| Trial ID | ACTRN12612000101886 |
|---|---|
| Public title | Evaluation of the Radioprotective Effect of Famotidine Against Radiotherapy- induced Acute Toxicity in Patients with Prostate Cancer |
| Scientific title | A Randomized controled trial of Famotidine as a Radioprotector agent versus Placebo before External Beam Radiotherapy in Patients with Prostate Cancer to Reduce Radiation- induced Acute Bowel & Urinary Toxicity using RTOG Criteria |
| Primary sponsor | School of Paramedical Sciences, Shahid Beheshti Medical University, |
| Secondary sponsors | Abolfazl Razzaghdoust |
| Registry | Australian New Zealand Clinical Trials Registry (ANZCTR) |
| Recruitment status | Not Recruiting |
| Study type | Interventional |
| Phase | Phase 1 / Phase 2 |
| Countries | Iran, Islamic Republic Of |
| Conditions | Prostate Cancer;Bowel toxicity;Urinary toxicity; Prostate Cancer Bowel toxicity Urinary toxicity;Cancer - Prostate;Oral and Gastrointestinal - Normal oral and gastrointestinal development and function;Renal and Urogenital - Normal… |
| Interventions | Oral Famotidine 40mg is administrated daily for 2 months twice per day before 2 months Radiotherapy: Once 4 hours before and the other 3 hours before daily Radiotherapy. A Physician determines Bowel & Urinary Toxicities Grade for the… |
| Registration date | Jan 20, 2012 |
| Target size | 36 |
| Secondary IDs | Nil |
| Registry page | anzctr.org.au |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: