EUCTR2009-011382-80-GBActive, not recruitingPhase 1
Intravenous Iron: biomarkers and treatment strategies in anaemic Colorectal cancer patients. - Intravenous Iron: measuring response in anaemic surgical patients
ottingham University Hospital0 sites20 target enrollmentStarted: May 8, 2009Last updated:
Conditions
Drugs
Trial Snapshot
- Phase
- Phase 1
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 20
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
Inclusion Criteria
- •Age >18yrs
- •Diagnosis of Colorectal Cancer and a defined surgical operation date
- •Biochemically detectable anaemia.
- •Women of child bearing potential (who have a negative pregnancy
- •test) must agree to use methods of medically acceptable forms of contraception during the study; (e.g. intra-uterine device (IUD) or a double-barrier method of oral contraception with condom)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
Exclusion Criteria
- •Patients with a recognised allergy to intravenous iron, or related products.
- •A concurrent medical condition(s) that,in the view of the investigator, would prevent compliance or participation or jeopardize the health of the patients.
- •Any of the following groups:
- •Children; those unable to consent for themselves; pregnant females; prisoners
Investigators
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