drugset / Trial / NCT01623206

Desmopressin (DDAVP) in Patients With Colorectal Cancer and Rectal Bleeding

NCT01623206

Phase 2 Completed 30 enrolled Laboratorio Elea Phoenix S.A.
NaSingle-groupOpen-labelOther

Summary

The objective of this study is to find the maximum tolerated dose and preliminary efficacy of desmopressin as an haemostatic agent, when is administered to patients with colorectal cancer and rectal bleeding, before specific oncologic treatment with surgery and/or chemotherapy and/or radiotherapy.

Timeline

Start
2013-04
Primary completion
2017-07
Completion
2017-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Desmopressin Peptide 0.25 ug/kg Intravenous
Subject Desmopressin Peptide 0.5 ug/kg Intravenous
Subject Desmopressin Peptide 1 ug/kg Intravenous
Subject Desmopressin Peptide 2 ug/kg Intravenous

Indications