Clinical Trials Directory

Trials / Completed

CompletedNCT01444456

Assessment of Quality of Life in Patients With Symptomatic Chemotherapy-induced Anaemia

Electronic Assessment of Quality of Life in Patients With Symptomatic Chemotherapy-induced Anaemia: An International Prospective Observational Study (eAQUA)

Status
Completed
Phase
Study type
Observational
Enrollment
1,262 (actual)
Sponsor
Amgen · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a multicenter, international, prospective, observational study of patients who are receiving systemic chemotherapy for solid tumour cancers (breast, colorectal, ovarian, prostate, lung, bladder, endometrial, renal, pancreatic, esophageal or gastric) and who are receiving darbepoetin alfa (Aranesp®) or other erythropoiesis-stimulating agent (ESA) to treat symptomatic anaemia. Quality of Life will be assessed electronically with the aim of estimating improvement in quality of life for those patients receiving darbepoetin alfa (Aranesp®) who also have an increase in haemoglobin (Hb) of ≥1 g/dL

Detailed description

Before enrolling participants, each country was assigned to either cohort 1 (patients receiving only darbepoetin alfa) or cohort 2 (patients receiving any ESA). Cohort 2 was assigned only to those countries in which local regulations did not permit observational study participation by patients receiving a specific agent in a drug class.

Conditions

Timeline

Start date
2011-10-01
Primary completion
2013-08-01
First posted
2011-09-30
Last updated
2017-03-20
Results posted
2014-08-15

Locations

117 sites across 9 countries: Austria, Belgium, France, Germany, Greece, Italy, Netherlands, Poland, Romania

Source: ClinicalTrials.gov record NCT01444456. Inclusion in this directory is not an endorsement.