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HUNGARIAN NON-INTERVENTIONAL STUDY TO OBSERVE THE TREATMENT OF SYMPTOMATIC ANAEMIA IN CANCER PATIENTS RECEIVING CHEMOTHERAPY AND NEORECORMON


N/A
18 Years
N/A
Not Enrolling
Both
Anemia

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Trial Information

HUNGARIAN NON-INTERVENTIONAL STUDY TO OBSERVE THE TREATMENT OF SYMPTOMATIC ANAEMIA IN CANCER PATIENTS RECEIVING CHEMOTHERAPY AND NEORECORMON


Inclusion Criteria:



- Adult patients, >/= 18 years of age

- Patients with solid tumors or lymphoproliferative disease

- Patients receiving chemotherapy

- Patients for whom erythropoietin is indicated for pre-study hemoglobin level and
observed anemic symptoms: Hgb < 11 dL (6.83 mmol/L)

Exclusion Criteria:

- Resistant hypertension

- Acute chronic bleeding within 3 months

- Iron deficiency, unmanageable prior to study

- Hypersensitivity to the active substance or any of the excipients of the product

- Pregnant or breast-feeding women

- Epoetin treatment within 6 months prior to study

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

Change in hemoglobin levels

Outcome Time Frame:

from baseline to end of treatment

Safety Issue:

No

Principal Investigator

Clinical Trials

Investigator Role:

Study Director

Investigator Affiliation:

Hoffmann-La Roche

Authority:

Hungary: Medical Research Council

Study ID:

ML21420

NCT ID:

NCT01809314

Start Date:

April 2008

Completion Date:

February 2012

Related Keywords:

  • Anemia
  • Anemia

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