Study Complete
Sponsor ID
20101123

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

Sponsor ID
20101123
Clinicaltrials.gov ID
NCT01444456
EUCTIS ID
N/A
EudraCT ID
N/A

Study Details

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

Additional Study Details

Phase
N/A
Product
darbepoetin alfa
Type
Observational
Masking
N/A
Enrollment
1262
Additional Study Details

Protocol Summary

Primary Outcome Measures

Proportion of subjects receiving darbepoetin alfa with improvement in Patient Perceived Fatigue (PPF) and increase in Hb >=1 g/dL

Timeframe: From Baseline to Week 9

Secondary Outcome Measures

Proportion of subjects by tumour type with improvement in Patient Perceived Fatigue (PPF) and increase in Hb >=1 g/dL

Timeframe: From Baseline to Week 9

Study Documents

Study Synopsis
Available Language(s): English

Locations

Location
Status
Contact Us
Location
Research Site
St Poelten, Austria, 3100
Status
Completed
Location
Research Site
Innsbruck, Austria, 6020
Status
Completed
Location
Research Site
Gilly, Belgium, 6060
Status
Completed
Location
Research Site
Oostende, Belgium, 8400
Status
Completed
Location
Research Site
Mechelen, Belgium, 2800
Status
Completed
Location
Research Site
Verviers, Belgium, 4800
Status
Completed
Showing {first} - {last} of {total} Results