Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 2:39 PM
Ignite Modification Date:
2025-12-26 @ 2:39 PM
NCT ID:
NCT01623206
Eligibility Criteria:
Inclusion Criteria:
* Patients \> 18 to \< 80 years of age who have signed the informed consent form
* Histological diagnosis of rectal adenocarcinoma localized, locally advanced or metastatic
* Treatment indication with chemotherapy and/or radiotherapy and/or surgery according to disease stage
* Rectal bleeding associated with the primary tumor within 48 hours prior to study entry
* Acceptable organ function to be able to participate in the study, performed within 14 days prior to admission; defined by the following parameters:
* Electrocardiogram (ECG) without significant clinical abnormalities
* Haemoglobin greater than or equal to 8 g/dL
* Total leukocyte count greater than or equal to 4.0 x 10\^9/L
* Absolute neutrophil count greater than or equal to 1.5 x 10\^9/L
* Total platelet count greater to 100.0 x 10\^9/L
* Total bilirubin less than or equal to 1.5 times the upper limit of normality (ULN)
* Serum glutamic oxaloacetic transaminase (SGOT) and serum glutamic pyruvic transaminase (SGPT) less than or equal to 1.5 times upper limit of normality (ULN)
* Creatinine clearance greater than 50 ml/min
* Performance status (Eastern Cooperative Oncology Group \[ECOG\]) less than or equal to 2
* Patients with childbearing potential should use one of the following contraceptives methods: intrauterine devices, barrier methods and tubal ligation
Exclusion Criteria:
* Colorectal cancer without bleeding evidences
* Pregnancy or lactation
* Use of hormonal contraceptives or treatments with sexual hormones in general
* Patients with other illnesses not adequately controlled such as congestive heart failure, arterial blood pressure, unstable angina, severe cardiac arrhythmia, thromboembolic disease, diabetes 1 or 2, any hidden coronary disease determined by previous assessments
* Psychiatric diseases implying patient incompetence
* Known hypersensitivity to desmopressin or vasopressin
* Severe von Willebrand disease (vWD)(defined by vWF\<10% Ui/dl) or 2B vWD (defined by increased platelet agregation induced by ristocetin at low concentration) or hemophilia A or B carriers
* History of seizures
* Renal insufficiency (Creatinine clearance \< 50 ml/min), hyponatremia (serum sodium lower than the lower limit of normality-UNL)or previous history of hyponatremia
* Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
* Positive serology for hepatitis B, C or known human immunodeficiency virus (HIV) infection
* Known liver disease (cirrhosis, liver enzymes greater than or equal to 1.5 times the upper limit of normality or total bilirubin greater than or equal to 1.5 times the upper limit of normality
* Active infections wich, according to the investigator judgement, coud interfere with patient safety
* Other malignancies, with the exception of basal cell carcinoma, in situ cervical carcinoma, or any other tumour adequately treated and with a disease-free period greater than or equal to 5 years
* Patients receiving or having received other investigational drugs 30 days prior to study entry
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT01623206
Study Brief:
Protocol Section:
NCT01623206